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Tuberculomas are rare and a life-threatening condition. Diagnosis followed by appropriate treatment can lead to complete resolution of the disease. A suggestive imaging study in an appropriate clinical setting can lead to the diagnosis. We describe a case of a postpartum woman with a headache and seizure in which eclampsia was the initial suspicion. Imaging exams demonstrated a solitary expansile lesion in the left parietal lobe suspicious of neoplasia. A biopsy, instead, confirmed a tuberculoma. In addition to eclampsia, many other differential diagnoses are possible in the context of seizures in pregnant and peripartum patients, including central nervous system tuberculosis. Brain imaging studies can be crucial in the diagnostic process.
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RESUMEN Una de las formas del cuadro inflamatorio-infeccioso de la tuberculosis, problema mayor de salud pública en América Latina, Asia y África y con potencial extensión mundial, es la forma parenquimal tumoral en el encéfalo, conocida como granuloma tuberculoso o tuberculoma. Este cuadro condiciona comúnmente efectos de masa y edema perilesional, los cuales suelen confundirse con manifestaciones radiológicas de otros granulomas y masas neoplásicas, en especial, las de alto grado. Son por ello necesarios estudios minuciosos de carácter clínico, epidemiológico, exámenes de laboratorio y, sobre todo, de imágenes por resonancia magnética. Se comparten en este artículo algunas observaciones de imágenes de casos comprobados de granuloma tuberculoso en el encéfalo, en pacientes examinados en un centro privado de diagnóstico radiológico por resonancia magnética en Lima. Los hallazgos podrían ayudar en el diagnóstico relativamente temprano de casos, previniéndose así el avance de la enfermedad y sus consecuencias, así como el empleo de métodos diagnóstico-terapéuticos invasivos.
ABSTRACT One of the forms of the inflammatory-infectious condition of tuberculosis, a major public health problem in Latin America, Asia and Africa with a potential worldwide spread, is the parenchymal tumor form in the brain, known as tuberculous granuloma or tuberculoma. This form commonly induces a mass effect and perilesional edema, which are often confused with the radiological manifestations of other granulomas and neoplastic masses, especially high-grade ones. Therefore, it is necessary to conduct careful clinical and epidemiological studies, laboratory tests and, above all, magnetic resonance imaging explorations. In this article, we share some MRI observations of proven cases of tuberculous granulomas in the brain, in patients seen at an MRI diagnostic radiological center. The findings could help in a relatively early diagnosis of cases, thus preventing the progression of the disease with its well-known consequences, and the use of invasive diagnostic/therapeutic methods.
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ABSTRACT Interstitial keratitis is an inflammation of the corneal stroma without epithelium or endothelium involvement. The underlying causes are mostly infectious or immune mediated. Brazil has one of the highest incidence rates of tuberculosis in the world. Tuberculosis is considered one of the causes of interstitial keratitis. Malnutrition and anemia are risk factors of the disseminated disease. This is a case report of a 10-year-old child who presented with decreased visual acuity and a clinical diagnosis of bilateral interstitial keratitis and sclero-uveitis. The patient had been treated with topical steroids with partial improvement. Examinations revealed severe iron deficiency anemia, negative serologies for human immunodeficiency virus and syphilis, positivity for cytomegalovirus- and herpes simplex-specific IgG, and purified protein derivative of 17 mm. During the follow-up, the patient presented with tonic-clonic seizures, and magnetic resonance imaging findings suggested a central nervous system tuberculoma. Interstitial keratitis improvement was observed after specific tuberculosis treatment. This is the first case report describing the association of interstitial keratitis and central nervous system tuberculoma.
RESUMO A ceratite intersticial é uma inflamação do estroma corneano sem envolvimento epitelial ou endotelial causada principalmente por doenças infecciosas e imunomediadas. O Brasil tem altas taxas de tuberculose que deve ser lembrada como causa de ceratite intersticial. Desnutrição e anemia são fatores de risco da forma disseminada da tuberculose. Este é um relato de uma criança de 10 anos com redução de acuidade visual e diagnóstico clínico de ceratite intersticial bilateral e esclerouveíte. O paciente obteve melhora parcial da ceratite com corticoide tópico. Exames laboratoriais mostraram anemia ferropriva grave, sorologias negativas para HIV e sífilis; IgM negativo e IgG positivo para citomegalovírus e herpes simplex e PPD positivo (17 mm). Ele evoluiu com crises tônico-clônicas e a ressonância nuclear magnética revelou tuberculoma do sistema nervoso central. A melhora da ceratite intersticial foi observada após tratamento para tuberculose. Este é o primeiro caso que descreve a associação de ceratite intersticial e tuberculoma do sistema nervoso central.
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INTRODUCTION: Heart transplantation is the standard treatment for end-stage heart disease. Despite advances in the field, patients remain under risk of developing complications, including opportunistic infections, such as tuberculosis. We present the unprecedented case of cerebral tuberculoma in a 9-year-old heart transplant recipient. CASE SCENARIO: A 9-year-old female child, who underwent heart transplantation in December 2020, was admitted to the emergency department in September 2021 due to headache and vomiting. She had normal vital signs and a mild left hemiparesis. Laboratory findings included lymphopenia and a low C Reactive Protein and brain images showed expansive lesions. A biopsy of the intracranial lesion was performed and anatomopathological analysis was compatible with tuberculoma. After the diagnosis was established, treatment protocol for neurotuberculosis was initiated, the patient had a satisfactory clinical evolution and was discharged 22 days after admission. DISCUSSION: Clinical manifestation of tuberculosis usually occurs up to 6 months after transplantation, the findings are commonly atypical and symptoms may be mild. We could not find in medical literature any description of the disease in a heart transplant recipient as young as the one presented in this case report. We documented great response to treatment, even though conventional antituberculosis therapy may interfere with immunosuppression. CONCLUSION: Patients in the postoperative period following heart transplantation are at high risk for developing opportunistic infections such as tuberculosis, which may present with atypical symptoms. Therefore the clinician must have a high index of suspicion in order to make the correct diagnosis and promptly start treatment.
Assuntos
Infecções Oportunistas , Tuberculoma Intracraniano , Tuberculose , Feminino , Humanos , Criança , Tuberculoma Intracraniano/diagnóstico , Tuberculoma Intracraniano/tratamento farmacológico , Tuberculoma Intracraniano/patologia , Encéfalo/diagnóstico por imagem , Encéfalo/patologiaRESUMO
Tuberculosis is one of the main causes of death due to infection around the world. Although tuberculosis frequently involves lung parenchyma, tuberculoma is a rare complication. We describe an atypical pulmonary presentation of tuberculosis. A 15-month-old girl, previously healthy, was referred to the pulmonology department due to fever, poor weight gain, and a 2-months persistent lung image on chest x-ray despite antibiotic therapy. She had been in frequent contact with a respiratory symptomatic subject. She was admitted to the hospital with a TST of 13 mm and a heterogeneous bulky mass in the left upper lobe at chest computed tomography. Three gastric lavages were Masa pulmonar como manifestación primaria de tuberculosis en pediatría: reporte de un caso Pulmonary tuberculosis presenting as a lung mass in children: case report done and the patient underwent exploratory thoracoscopy and lung biopsy, with positive cultures for Mycobacterium tuberculosis. The diagnosis of pulmonary tuberculoma was confirmed, and the patient received standard anti- tuberculosis therapy with a favorable evolution.
La tuberculosis es una de las principales causas infecciosas de muerte en el mundo y es endémica en Argentina. La mayoría de los casos de tuberculosis son de localización pulmonar; el tuberculoma una complicación infrecuente. Se describe un caso clínico de presentación pulmonar atípica de tuberculosis. Se trata de una niña de 15 meses, previamente sana, derivada a neumología por fiebre, mal progreso de peso e imagen persistente por 2 meses en la radiografía de tórax a pesar de haber recibido antibioticoterapia. Antecedente de contacto estrecho con persona sintomática respiratoria. Se internó para estudio, mostró una PPD de 13 mm y una masa voluminosa heterogénea en el lóbulo superior izquierdo en la tomografía computada de tórax. Se realizaron tres lavados gástricos y toracoscopia exploratoria con biopsia pulmonar con rescate de Mycobacterium tuberculosis en cultivos. Se diagnosticó tuberculoma pulmonar y realizó tratamiento estándar con fármacos antituberculosos con evolución favorable.
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Tuberculoma , Tuberculose dos Linfonodos , Tuberculose Pulmonar , Antibacterianos , Criança , Feminino , Humanos , Lactente , Pulmão/patologia , Tuberculoma/patologia , Tuberculose Pulmonar/complicações , Tuberculose Pulmonar/diagnósticoRESUMO
La tuberculosis es una de las principales causas infecciosas de muerte en el mundo y es endémica en Argentina. La mayoría de los casos de tuberculosis son de localización pulmonar; el tuberculoma una complicación infrecuente. Se describe un caso clínico de presentación pulmonar atípica de tuberculosis. Se trata de una niña de 15 meses, previamente sana, derivada a neumología por fiebre, mal progreso de peso e imagen persistente por 2 meses en la radiografía de tórax a pesar de haber recibido antibioticoterapia. Antecedente de contacto estrecho con persona sintomática respiratoria. Se internó para estudio, mostró una PPD de 13 mm y una masa voluminosa heterogénea en el lóbulo superior izquierdo en la tomografía computada de tórax. Se realizaron tres lavados gástricos y toracoscopia exploratoria con biopsia pulmonar con rescate de Mycobacterium tuberculosis en cultivos. Se diagnosticó tuberculoma pulmonar y realizó tratamiento estándar con fármacos antituberculosos con evolución favorable.
Tuberculosis is one of the main causes of death due to infection around the world. Although tuberculosis frequently involves lung parenchyma, tuberculoma is a rare complication. We describe an atypical pulmonary presentation of tuberculosis. A 15-month-old girl, previously healthy, was referred to the pulmonology department due to fever, poor weight gain, and a 2-months persistent lung image on chest x-ray despite antibiotic therapy. She had been in frequent contact with a respiratory symptomatic subject. She was admitted to the hospital with a TST of 13 mm and a heterogeneous bulky mass in the left upper lobe at chest computed tomography. Three gastric lavages were done and the patient underwent exploratory thoracoscopy and lung biopsy, with positive cultures for Mycobacterium tuberculosis. The diagnosis of pulmonary tuberculoma was confirmed, and the patient received standard anti- tuberculosis therapy with a favorable evolution.
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Humanos , Feminino , Lactente , Tuberculoma/patologia , Tuberculose dos Linfonodos , Tuberculose Pulmonar/complicações , Tuberculose Pulmonar/diagnóstico , Pulmão/patologia , AntibacterianosRESUMO
ABSTRACT Choroidal tuberculomas are present in patients with ocular tuberculosis. They usually occur in a patient with previous history of tuberculosis, and are rarely the initial presentation, with no prior systemic manifestations. We present a patient with unilateral choroidal tuberculoma as the initial presentation of presumed ocular tuberculosis, which enabled earlier initiation of treatment.
RESUMO Os tuberculomas de coroide apresentam-se em pacientes com tuberculose ocular. Geralmente, ocorrem em indivíduos com história prévia de tuberculose e raramente têm apresentação inicial sem manifestações sistêmicas anteriores. Relatamos o caso de um paciente com tuberculoma de coroide unilateral com apresentação inicial de tuberculose ocular presumida, permitindo o início mais precoce do tratamento.
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Humanos , Feminino , Adulto , Tuberculoma/diagnóstico , Doenças da Coroide/diagnóstico , Tuberculoma/tratamento farmacológico , Angiofluoresceinografia , Doenças da Coroide/tratamento farmacológico , Uveíte Posterior/diagnóstico , Tuberculose Ocular , Corioide/diagnóstico por imagem , Fundo de Olho , Antituberculosos/uso terapêuticoRESUMO
Tuberculosis (TB) of the central nervous system (CNS) is considered one of the most severe forms of presentation of the disease. Although only 1% of TB cases involve the CNS, these cases represent around between 5 and 15% of extrapulmonary forms.1,2 Tuberculous meningitis (TBM) is the most frequent form of CNS TB. The granulomas formed in the cerebral tuberculoma may cause hydrocephalus and other symptoms indicative of a CNS mass lesion. In the absence of active TB or TBM, the symptoms may be interpreted as indicative of tumors.3,4 The prognosis is directly related to the early diagnosis and proper treatment installation.5 We report the case of a patient with intracranial hypertension syndrome, expansive mass in the parieto-occipital region, accompanied by a lesion in the rib, initially thought to be a metastatic lesion, although posteriorly diagnosed as a cerebral tuberculoma.
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Humanos , Masculino , Idoso de 80 Anos ou mais , Tuberculoma/diagnóstico , Tuberculoma/terapia , Tuberculoma Intracraniano/patologia , Tuberculose do Sistema Nervoso Central , Microcirurgia/métodos , Antituberculosos/uso terapêuticoRESUMO
RESUMEN Introducción: El síndrome de Otelo, epónimo del personaje de Shakespeare, es un término diagnóstico transnosológico que designa un cuadro caracterizado por delirios de infidelidad respecto a la pareja que, por consiguiente, puede acarrear actitudes celotípicas y conductas violentas hacia ella. En su forma pura, corresponde al trastorno delirante de infidelidad, pero también puede ser secundario a organicidad cerebral y a consumo de drogas. Métodos: Reporte de caso y revisión no sistemática de la literatura relevante. Presentación del caso: Varón de 26 arios con antecedente de consumo de drogas y víctima de maltrato infantil, 3 años antes había sufrido crisis convulsivas tónico-clónicas e hipertensión intracraneal, por lo que se sometió a una craneotomía, en la que se halló un tuberculoma cerebral frontal derecho. Tras un lapso, comenzó con delirios de infidelidad y conductas violentas hacia su pareja. Revisión de la literatura: Los celos delirantes se asocian, como otros delirios, a lesiones del lóbulo frontal derecho. Pese a la elevada y creciente prevalencia mundial de tuberculosis, no se han publicado casos de síndrome de Otelo secundario a tuberculoma cerebral. Conclusiones: El síndrome de Otelo, aunque no es la principal causa de violencia doméstica, puede asociarse con manifestaciones particularmente violentas y ser secundario a tuberculoma cerebral. Este es el primer caso de tal índole que se publica.
ABSTRACT Introduction: Othello syndrome, an eponym of Shakespeare's character, is a transnosological diagnostic term that designates a clinical picture characterised by the presence of delusions of infidelity with respect to a partner and that, consequently, can lead to typical jealousy attitudes and violent behaviour towards the partner. In its pure form, it corresponds to delusional disorder of infidelity, but it may also be secondary to brain organicity and drug use. Methods: Case report and non-systematic review of the relevant literature. Case presentation: A 26-year-old man, with a history of drug abuse and a victim of domestic violence as a child, presented with tonic-clonic seizures and intracranial hypertension three years ago, for which he underwent a craniotomy with the finding of a right frontal cerebral tuberculoma. After a lapse, he developed a clinical picture of delusions of infidelity regarding his partner and violent behaviour towards her. Literature review: Delusional jealousy is associated, like other delusions, with lesions of the right frontal lobe. Despite the high and growing prevalence of tuberculosis worldwide, there are no reported cases of Othello syndrome secondary to cerebral tuberculoma in the literature. Conclusion: Othello syndrome, although not the main cause of domestic violence, can be associated with particularly violent manifestations and be secondary to cerebral tuberculoma. This is the first published case of its kind.
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Humanos , Masculino , Adulto , Síndrome , Transtornos Relacionados ao Uso de Substâncias , Ciúme , Esquizofrenia Paranoide , Convulsões , Atitude , Prevalência , Violência Doméstica , Hipertensão Intracraniana , Craniotomia , Diagnóstico , Epônimos , Lobo FrontalRESUMO
Meningitis or meningoencephalitis are the most common presentations of Koch bacilli infection on the central nervous system (CNS), especially in immunosuppressed patients, in whom the bacilli normally reaches the meninges and the cerebral parenchyma.. A least common pathological presentation is the tumoral growth pattern disease known as tuberculoma. This pathological entity is more common in the cerebral hemispheres and is rarely located in the brainstem. The present case report describes a case of a 55-year-old patient under regular antiretroviral therapy who was hospitalized with signs of brainstem and cerebellar disturbances. Computed tomography (CT) and magnetic resonance imaging (MRI) of the brain showed an exophytic lesion in the dorsal region of the pons. The patient underwent total resection of the lesion and the histopathologic analysis was consistent with a tuberculoma.
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Humanos , Masculino , Pessoa de Meia-Idade , Tuberculoma/patologia , Tuberculose Meníngea/diagnóstico , Tuberculose Meníngea/terapia , Tronco Encefálico/patologia , Hospedeiro ImunocomprometidoRESUMO
Resumen La tuberculosis (TBC) cerebral o tuberculoma(s) sin meningitis es una enfermedad poco frecuente y de alta morbimortalidad. Presentamos el caso clínico de un lactante de 11 meses, previamente sano, que consultó por fiebre prolongada y síntomas neurológicos. La RM de encéfalo mostró múltiples imágenes micronodulares e hidrocefalia. El estudio de LCR para bacterias, hongos y micobacterias fue negativo. Se prescribió terapia empírica como una meningoencefalitis subaguda y tratamiento antituberculoso tetraconjugado y corticoesteroides. La confirmación del diagnóstico de TBC cerebral se realizó por biopsia de la lesión, con presencia de inflamación granulomatosa crónica necrosante y bacilos ácido-alcohol resistentes. Se enfatiza la importancia de considerar esta presentación de TBC en niños, y la necesidad de la búsqueda exhaustiva del agente etiológico en diferentes líquidos y tejidos, aun por métodos invasores.
Cerebral tuberculosis TB (tuberculomas) without meningitis is an uncommon disease with a high morbidity and mortality. We report on a case that illustrates the complexity of this clinical presentation. An 11 month old, previously healthy male infant was brought to the clinic due to fever present during the last 1.5 months, associated with loss of neurodevelopmental goals and signs of endocranial hypertension. CT scan of the skull revealed dilatation of the ventricular system with transependimary edema; MRI showed multiple intra- and extra-axial micronodular images and hydrocephalus. Studies of CSF (cyto-chemical analysis, staining, culture for aerobes, fungi, mycobacteria, and molecular tests for TB were negative). Empirical management for subacute meningoencephalitis was prescribed complemented with tetraconjugated treatment for TB and steroids. As there was no microbiological isolation, biopsy of a cerebellar lesion was performed, which revealed chronic necrotizing granulomatous inflammation and acid-alcohol resistant bacilli. The diagnosis of cerebral TB without meningeal involvement was confirmed. The objective of the present report is to emphasize the importance of considering this presentation of TB in children, to remark the need of exhaustive search for the etiologic agent by obtaining samples of the different fluids and tissues even if it implies recurring to invasive methods.
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Humanos , Masculino , Lactente , Tuberculose Meníngea/patologia , Tuberculoma Intracraniano/patologia , Tuberculose Meníngea/tratamento farmacológico , Biópsia , Imageamento por Ressonância Magnética , Radiografia Torácica , Tomografia Computadorizada por Raios X , Tuberculoma Intracraniano/tratamento farmacológico , Combinação Amoxicilina e Clavulanato de Potássio/uso terapêutico , Diagnóstico Diferencial , Imunocompetência , Meningoencefalite/diagnóstico , Antituberculosos/uso terapêuticoRESUMO
La tuberculosis es una de las enfermedades infecciosas más frecuentes de distribución mundial, con una amplia presentación clínica. La afectación hepática de la tuberculosis es poco frecuente, pero más infrecuente aún lo es el tuberculoma hepático. Se presenta el caso de una paciente con tuberculoma hepático solitario que simula metástasis hepática secundaria a tumor neuroendocrino
Tuberculosis is one of the most common infectious diseases, with worldwide distribution and ample clinical manifestations. Hepatic tuberculosis is rare but hepatic tuberculoma is even rarer. We report an unusual case of a solitary hepatic tuberculoma simulating hepatic metastasis of a neuroendocrine tumor
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Humanos , Mycobacterium tuberculosis , Tuberculoma , Tuberculose Hepática , Hiperplasia Nodular Focal do FígadoRESUMO
El sistema nervioso central es uno de los focos extrapulmonares afectados con mayor frecuencia por tuberculosis, no obstante, el tuberculoma epidural espinal es considerado una rareza. Se presenta el caso de un paciente de cuatro años de edad, quien consulta por cuadro de cuadriparesia progresiva. Al examen de líquido cefalorraquídeo se evidenció disociación proteínico celular diagnosticándose síndrome de Guillain Barré, sin embargo, tras la aparición de signos meníngeos, se realizó una resonancia nuclear magnética de columna en la que se evidenció lesión compresiva a nivel cervicodorsal que fue posteriormente explorada quirúrgicamente por neurocirugía, encontrándose una lesión epidural cuyo estudio microbiológico, cultivo y estudio de reacción en cadena de la polimerasa se reportaron positivos para Mycobacterium tuberculosis, por lo que se inició tratamiento antituberculoso observándose mejoría clínica y progresiva con recuperación de la marcha tras el procedimiento quirúrgico. MÉD.UIS. 2016;29(2):155-9.
The central nervous system is one of the most affected focus in extrapulmonary tuberculosis, however, spinal epidural tuberculoma is considered very unusual. We present a clinical report of a four years old patient who presented with clinical symptoms of a progressive quadriparesis. The cerebroespinal fluid examination showed protein-cell dissociation, and the diagnosis of Guillain Barré syndrome was made. However, because it called the attention the appearance of meningeal signs, a magnetic resonance imaging was performed, and evidenced a compressive lesion in the cervicodorsal level. It was explored by neurosurgery, finding an epidural lesion studied by cultures and polymerase chain reaction. Both reported positive results for Mycobacterium tuberculosis. The anti-tuberculosis treatment was started and a progressive clinical improvement was observed with recuperation of the gait after the surgical procedure.MÉD.UIS. 2016;29(2):155-9.
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Humanos , Masculino , Pré-Escolar , Tuberculoma , Sistema Nervoso Central , Tuberculose , Síndrome de Guillain-Barré , Sistema NervosoRESUMO
Resumen Se describe el caso de un paciente masculino de 35 años de edad, que se presenta con un tuberculoma intramedular torácico, con diagnóstico de VIH (Virus de la inmunodeficiencia humana) de seis años de evolución y dos meses antes TB (tuberculosis) pulmonar; su manejo médico y HAART (terapia antirretroviral altamente efectiva) sin adecuada adherencia. Se describe la contribución al diagnóstico de la RM (resonancia magnética), en la cual se visualiza área de mielitis focal en T10 que se marca intensamente con el medio de contraste, imagen que sugiere infección por TB. El tuberculoma intramedular es raro, pero debe ser considerado como diagnóstico diferencial de síntomas compresivos medulares en pacientes infectados por VIH, de evolución no clara y estudios del líquido cefalorraquídeo negativos. (Acta Med Colomb 2016; 41: 141-143).
Abstract The case of a 35 years old male patient with a thoracic intramedullary tuberculoma, with diagnosis of HIV (Human Immunodeficiency Virus) of six years of evolution and of pulmonary TB (tuberculosis) two months before, is presented; he had medical management and HAART (highly effective anti retroviral therapy) without proper adhesion. The contribution of MRI (magnetic resonance imaging) to the diagnosis, in which an image of focal area of myelitis in T10 intensely marked with contrast medium, suggests TB infection, is described. The intramedullary tuberculoma is rare, but should be considered as a differential diagnosis of symptoms of spinal cord compression in HIV-infected patients with no clear evolution and negative cerebrospinal fluid studies. (Acta Med Colomb 2016; 41: 141-143).
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Humanos , Masculino , Adulto , Tuberculoma , Tuberculose , Espectroscopia de Ressonância Magnética , Sistema Nervoso CentralRESUMO
RESUMEN La tuberculosis con afección del sistema nervioso central es una afectación infrecuente pero muy grave de esta enfermedad, representa el 1% de todos los casos de tuberculosis. Reportamos el caso de una joven HIV negativa, con daño del sistema nervioso central de tipo miliar a nivel cerebral y sin enfermedad pulmonar. La tuberculosis puede afectar extensamente a sujetos inmunocompetentes y este fenómeno ha sido descripto en muchas series a los largo del tiempo. Ante la sospecha clínica, el seguimiento de un protocolo específico para confirmar el diagnóstico es de vital importancia para el temprano diagnóstico y correcto manejo de una situación que puede comprometer la vida y generar a largo plazo secuelas graves. Se presenta el caso por el reto diagnóstico que ha supuesto y rara presentación en paciente inmunocompetente.
ABSTRACT Tuberculosis with central nervous system involvement is an uncommon but very serious disease, with a frecuence of 1% of all cases of tuberculosis. We report the case of a young HIV negative woman, with central nervous system damage of the miliary type in the brain without lung disease. Tuberculosis can extensively affect immunecompetent subjects and this phenomenon has been described in many series over the time. In the presence of clinical suspicion, the follow-up of a specific protocol to confirm the diagnosis is of vital importance for the early diagnosis and correct management of a situation that can compromise life and generate long-term serious sequelae. The case is presented because of diagnostic challenge and a rare presentation in an immunocompetent patient.
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Humanos , Feminino , Adolescente , Encefalopatias/diagnóstico por imagem , Tuberculoma Intracraniano/diagnóstico por imagem , Encefalopatias/tratamento farmacológico , Imageamento por Ressonância Magnética , Cefalosporinas/uso terapêutico , Tuberculoma Intracraniano/tratamento farmacológico , Quinolonas/uso terapêutico , Imunocompetência , Antituberculosos/uso terapêuticoRESUMO
Tuberculosis is a chronic bacterial infection caused by Mycobacterium tuberculosis. Despite advances in treatment, resistant strains and unusual sites of involvement have been diagnosed. We present a case of a 13-year-old patient in treatment for tuberculous meningitis who presented with progressive paraparesis. The MRI showed two intramedullary nodular lesions at T4T6 levels, isointense with annular hyperintensity on T1W, hypointense on T2W, becoming hypointense with ring enhancement after contrast. These characteristics differ from those usually described for intramedullary tuberculomas. Surgical excision was performed, confirming the diagnosis of intramedullary tuberculoma. The formation of intramedullary tuberculomas is rare, with a ratio of two cases per thousand diagnosed with CNS tuberculosis, and the thoracic spine is most frequently affected. The clinical picture is of progressive subacute spinal cord compression, and it may lead to paraplegia. At MRI, the lesion in early stage appears as hypointense rings on T1W and hyperintense on T2W, with homogeneous enhancement after contrast. After the formation of the solid caseous granuloma, it becomes isointense on T1W and hypointense on T2W with homogeneous enhancement after contrast. When the center of the granuloma becomes liquefied, it shows hypointense sign on T1W and hyperintense with peripheral enhancement on T2W. The treatment of choice is medical, with the current protocol including rifampin, isoniazid, pyrazinamide, and ethambutol. Surgery is reserved for cases of progressive neurologic deficits or for diagnostic confirmation. Although benign and potentially curable, intramedullary tuberculoma should be promptly diagnosed and treated to prevent irreversible damage.
A tuberculose é uma infecção bacteriana crônica causada pelo Mycobacterium tuberculosis. Apesar dos avanços no tratamento, cepas resistentes e locais incomuns de envolvimento vêm sendo diagnosticados. Apresentamos o caso de um paciente de 13 anos de idade, em tratamento para meningite tuberculosa que se apresentou com paraparesia progressiva. A ressonância magnética mostrou duas lesões nodulares intramedulares no nível de T4T6, isointensas com bordos hiperintensos em T1, hipointensos em T2, tornando-se hipointensos com realce anelar após contraste. Essas características diferem daquelas usualmente descritas para tuberculomas intramedulares. Foi realizada a excisão cirúrgica, confirmando o diagnóstico de tuberculoma intramedular. A formação de tuberculomas intramedulares é rara, com uma proporção de dois casos por mil diagnosticados com tuberculose do sistema nervoso central (SNC), e a coluna torácica é a mais frequentemente acometida. O quadro clínico é de compressão da medula espinal progressiva subaguda, podendo levar à paraplegia. Na ressonância magnética, a lesão em fase inicial aparece como anéis hipointensos em T1 e hiperintensos em T2, com realce homogêneo após contraste. Após a formação do granuloma caseoso sólido, torna-se isointensa em T1 e hipointensa em T2, com realce homogêneo após contraste. Quando o centro do granuloma torna-se liquefeito, mostra sinal hipointenso em T1 e hiperintenso com realce periférico em T2. O tratamento de escolha é medicamentoso, com o protocolo corrente de rifampicina, isoniazida, pirazinamida e etambutol. A cirurgia é reservada para os casos de déficit neurológico progressivo ou para confirmação diagnóstica. Embora benigna e potencialmente curável, deve ser diagnosticada e tratada para evitar danos irreversíveis.
Assuntos
Humanos , Masculino , Adolescente , Tuberculose Meníngea/diagnóstico , Tuberculose Meníngea/terapia , Tuberculoma Intracraniano/diagnósticoRESUMO
A solitary tuberculous brain lesion (STBL) can be difficult to distinguish from a glioma, metastasis or other infectious disease, especially from a pyogenic brain abscess. We analyzed the clinical characteristics, diagnostic procedures and outcomes of 24 patients with STBL diagnosed in three centers from France, India and Mexico. We also reviewed 92 STBL cases previously reported in the literature. General symptoms were found in 54% of our patients, including enlarged lymph nodes in 20%. Cerebrospinal fluid was typically abnormal, with lymphocytic pleocytosis and a high protein level. The lung CT scan was abnormal in 56% of patients, showing lymphadenopathy or pachipleuritis. Brain MRI or CT was always abnormal, showing contrast-enhanced lesions. Typically, MRI abnormalities were hypointense on T1-weighted sequences, while T2-weighted sequences showed both a peripheral hypersignal and a central hyposignal. The diagnosis was documented microbiologically or supported histologically in 71% of cases. Clinical outcome was good in 83% of cases.
Assuntos
Tuberculoma Intracraniano/epidemiologia , Adolescente , Adulto , Idoso , Antituberculosos/uso terapêutico , Abscesso Encefálico/diagnóstico , Neoplasias Encefálicas/diagnóstico , Comorbidade , Diagnóstico Diferencial , Feminino , Febre/etiologia , França/epidemiologia , Glioma/diagnóstico , Cefaleia/etiologia , Humanos , Índia/epidemiologia , Imageamento por Ressonância Magnética , Masculino , México/epidemiologia , Pessoa de Meia-Idade , Marrocos/etnologia , Mycobacterium tuberculosis/isolamento & purificação , Avaliação de Sintomas , Tomografia Computadorizada por Raios X , Tuberculoma Intracraniano/diagnóstico , Tuberculoma Intracraniano/tratamento farmacológico , Tuberculoma Intracraniano/patologia , Tuberculose Pulmonar/diagnóstico por imagem , Tuberculose Pulmonar/epidemiologia , Adulto JovemRESUMO
RESUMEN Se presenta caso clínico de mujer joven con convulsiones, masa ocupante de espacio en cerebro y lesiones nodulares en pulmones. Se confirmó tuberculosis pulmonar por bacteriología y anatomía patológica. El tratamiento antituberculoso curó la afectación pulmonar también hizo remitir la lesión cerebral, confirmándose así un tuberculoma cerebral.
ABSTRACT We present a case of a young woman who presented with seizures, space-occupying mass nodular lesions in the brain and lungs. Pulmonary tuberculosis was confirmed with bacteriology and histopathology. Anti tuberculosis treatment cured lung lesions, also with remission of made forward brain lesion, confirming a tuberculoma of the brain.
RESUMO
Tuberculosis is an important public health problem. It is estimated that around 5-10% of patients with tuberculosis present with central nervous system involvement; meningitis and tuberculoma being two of the most frequent manifestations. The paradoxical reaction in patients undergoing antituberculosis treatment is infrequent, nevertheless it is an important consideration in patients, who after an appropriate initial response to specific treatment, present with worsening clinical and radiological signs or the appearance of new lesions.
La tuberculosis (TBC) es un problema de importancia en salud pública. Se estima que alrededor de 5 a 10% de los pacientes con TBC presentan compromiso de sistema nervioso central, siendo la meningitis y el tuberculoma las manifestaciones más frecuentes. La reacción paradojal en pacientes con tratamiento antituberculoso es infrecuente, sin embargo, es importante considerarla en pacientes que durante la terapia, luego de una respuesta inicial apropiada, presentan un empeoramiento clínico y/o radiológico o aparición de nuevas lesiones.
Assuntos
Adolescente , Feminino , Humanos , Antituberculosos/efeitos adversos , Tuberculose Meníngea/tratamento farmacológico , Tuberculose Pulmonar/tratamento farmacológico , Corticosteroides/uso terapêutico , Antituberculosos/uso terapêutico , Imunocompetência , Imageamento por Ressonância Magnética , Tuberculoma Intracraniano/tratamento farmacológico , Tuberculose Meníngea/diagnóstico , Tuberculose Pulmonar/diagnósticoRESUMO
BACKGROUND: Cavernous sinus tuberculomas are extremely rare, but the increasing incidence worldwide of central nervous system (CNS) tuberculosis, mostly due to human immunodeficiency virus and poor sanitary conditions, and the ability of tuberculomas to mimic a brain neoplasm makes cavernous sinus tuberculomas a suspicious pathologic finding in the differential diagnosis of a brain space-occupying lesion. CASE DESCRIPTION: We present an immunocompetent patient with no signs of systemic tuberculosis and an isolated right cavernous sinus space-occupying lesion. A skull base approach was performed and tumor resection achieved. The postoperative course was uneventful. Pathologic findings consisted of a tuberculoma and antituberculous treatment was immediately begun with total tumor regression after a 12-month regimen. After reviewing the literature, we propose suggestions to orient the diagnosis and a treatment algorithm for tuberculomas in rare locations. CONCLUSION: Tuberculomas in rare locations, as the cavernous sinus, are a challenging pathology as they have the ability to mimic a brain neoplasm. Although first line treatment are antituberculous therapy (4 drugs for at least 12 months) and adjuvant steroids, in inconclusive cases, surgical biopsy or excision is recommended for histopathologic confirmation and to reduce the mass effect, always following with antituberculous therapy and adjuvant steroids.