RESUMEN
Extrapulmonary small cell carcinoma (EPSCC) refers to small cell carcinoma arising outside of the lungs. EPSCC extrapulmonary small cell carcinoma is a rare aggressive neoplasm, representing a minority of all small cell carcinomas. Despite its uncommon occurrence, EPSCC extrapulmonary small cell carcinoma has been described in nearly every organ, most commonly in the gastrointestinal and genitourinary systems. As such, it is important for radiologists to be aware of the entity. Although imaging is neither sensitive nor specific for EPSCC extrapulmonary small cell carcinoma , it plays an important role by helping exclude metastases from a primary pulmonary tumor, establish tumor staging, and assess response to therapy. EPSCC extrapulmonary small cell carcinoma is diagnosed by demonstrating pathologic features of small cell carcinoma in an extrapulmonary site. There are two ways to stage EPSCC extrapulmonary small cell carcinoma . One method uses the Veterans Administration Lung Study Group system developed for small cell lung cancer that allocates patients into limited or extensive disease categories. The second approach is the American Joint Committee on Cancer tumor-node-metastasis system applied to other tumor subtypes arising from the same organ. Because of its rare and varied manifestations, the most effective treatment for EPSCC extrapulmonary small cell carcinoma has not been established. Current management recommendations are derived from retrospective studies and single-institution experiences or are extrapolated from small cell lung cancer data. Regardless of therapy, overall survival rates are poor, with 5-year survival rates around 13%. To help radiologists increase their familiarity with EPSCC extrapulmonary small cell carcinoma , this article provides (a) a background for EPSCC extrapulmonary small cell carcinoma based on the literature and (b) a pictorial review of EPSCC extrapulmonary small cell carcinoma in multiple organs, with radiologic-pathologic correlation.
Asunto(s)
Carcinoma de Células Pequeñas/diagnóstico , Diagnóstico por Imagen , Carcinoma de Células Pequeñas/epidemiología , Carcinoma de Células Pequeñas/patología , Medios de Contraste , Humanos , Estadificación de NeoplasiasRESUMEN
OBJECTIVE: To demonstrate the unique morphologic and phenotypic features observed in cases of T-cell lymphomas presenting as effusions. STUDY DESIGN: Cytologic slides and flow cytometric histograms of 8 cases of body fluids with T-cell lymphoma were retrospectively reviewed. Morphologic features, flow cytometric histograms and immunophenotypes of the cells were evaluated. RESULTS: Three of the 8 cases showed 1 or more of the following: intermediate-to-large cells with an increased nuclear-cytoplasmic ratio, finely granular or vacuolated cytoplasm and round or convoluted vesicular nuclei with a prominent single or multiple nucleoli. Flow cytometric studies of these 3 cases showed an abnormal scatter pattern in the myelomonocytic region of the histograms. Phenotypic analysis revealed variable expression of a T-cell phenotype. The remaining cases showed the conventional morphologic and flow cytometric features of a T-cell lymphoma. CONCLUSION: Morphologic alterations of neoplastic T-cells in body fluids can result in a variety of potentially incorrect diagnoses. The unusual flow cytometric histogram can serve as a useful clue for the diagnosis of T-cell lymphoma in body fluids but could be a potential pitfall for a false negative. Detailed cytologic evaluation combined with flow cytometric study can improve diagnostic accuracy.
Asunto(s)
Citodiagnóstico , Linfoma de Células T/patología , Anciano , Líquidos Corporales/citología , Citometría de Flujo , Humanos , Inmunohistoquímica , Masculino , Persona de Mediana Edad , FenotipoRESUMEN
Immunophenotypic study is critical for the diagnosis of adult small-round-cell tumors (SRCTs). We describe three patients with Ewing's sarcoma/primitive neuroectodermal tumor (ES/PNET) and one patient with neuroblastoma in which flow cytometry immunophenotyping (FCI) on the fine-needle aspirate (FNA) and bone marrow aspirate (BMA) demonstrated an abnormal population of cells that were CD45(-) and CD16/CD56(+). Four patients with mean age of 30 years, three male and one female, clinically suspicious for a lymphoma or SRCT are described. FNA, BMA, and biopsy specimens were obtained for routine cytologic and histologic evaluation. Fresh tissue was studied by FCI. In all cases, the cytology smears showed small cells with round nuclei, slightly irregular nuclear membranes, fine chromatin, and scant cytoplasm. FCI showed CD16/56(+) and CD45(-) neoplastic cells in all cases. In one case, 76% of these cells were CD99(+). The diagnoses of ES/PNET were confirmed by immunohistochemical, ultrastructural, and cytogenetic studies. ES/PNET in FNA and BMA can be efficiently and rapidly diagnosed by combining cytologic examination with FCI using a panel including CD45, CD16/56, and CD99.
Asunto(s)
Biopsia con Aguja Fina , Carcinoma de Células Pequeñas/patología , Citometría de Flujo , Tumores Neuroectodérmicos/patología , Antígeno 12E7 , Adolescente , Adulto , Antígenos CD/metabolismo , Médula Ósea/metabolismo , Médula Ósea/patología , Antígeno CD56/metabolismo , Carcinoma de Células Pequeñas/metabolismo , Carcinoma de Células Pequeñas/ultraestructura , Moléculas de Adhesión Celular/metabolismo , Femenino , Humanos , Inmunohistoquímica , Inmunofenotipificación , Antígenos Comunes de Leucocito/metabolismo , Masculino , Neuroblastoma/metabolismo , Neuroblastoma/patología , Neuroblastoma/ultraestructura , Tumores Neuroectodérmicos/metabolismo , Tumores Neuroectodérmicos/ultraestructura , Receptores de IgG/metabolismoRESUMEN
Myxoid neurothekeomas (nerve sheath myxomas) are rare benign cutaneous neoplasms that may morphologically mimic other myxoid neoplasms of skin and soft tissue. The cytologic and histopathologic features of this lesion may resemble various myxoid sarcomas, chordoma, myxoid neurofibroma, dermal cutaneous mucinosis, and cutaneous myxoma as well as other myxoid or chondroid neoplasms. In this study, a myxoid neurothekeoma was analyzed using multiple techniques. We found that myxoid neurothekeomas reveal a nonspecific pattern by fine-needle aspiration, including stellate cells embedded within an abundant metachromatic myxoid stromal matrix. These are cytologic features shared by various other subcutaneous neoplasms and thus may not be helpful in forming a definitive diagnosis. Histopathologically, the tumor is composed of nodules of myxoid stroma containing interspersed bland spindled and stellate cells. Immunohistochemical studies show tumor cell positivity for S-100 protein and vimentin, a profile shared by other neoplasms with similar cytologic features and therefore of little diagnostic value. The histologic and cytologic differential of subcutaneous and soft tissue myxomatous lesions is broad and, therefore, is of unique value to the cytopathologist to consider myxoid neurothekeomas among the differential of other myxomatous neoplasms.
Asunto(s)
Neurotecoma/metabolismo , Neurotecoma/patología , Neoplasias Nasales/metabolismo , Neoplasias Nasales/patología , Biopsia con Aguja , Desmina/metabolismo , Diagnóstico Diferencial , Humanos , Inmunohistoquímica , Queratinas/metabolismo , Masculino , Proteínas S100/metabolismo , Neoplasias de los Tejidos Blandos/metabolismo , Neoplasias de los Tejidos Blandos/patología , Vimentina/metabolismoRESUMEN
BACKGROUND: Lipoblastomas are rare tumors of embryonal fat that occur in infants and children. They are usually located in the extremities and trunk. Two cases in the parotid region have been described. A diagnosis on fine needle aspiration (FNA) specimens has been reported in six cases. CASE: Lipoblastoma of the parotid region occurred in a 6-year-old boy and was diagnosed by FNA. Cytology showed rare lipoblasts and hibernomalike cells in a myxoid background with spindle and stellate mesenchymal cells, mature adipose cells and plexiform capillaries. A 7.0-cm, well-circumscribed mass with lobulated adipose tissue and delicate fibrous bands was resected. Microscopically, it showed a lobulated myxoid stroma, many capillaries, mesenchymal cells, lipoblasts and mature adipose cells. CONCLUSION: Lipoblastoma has to be differentiated from myxoid and lipomatous soft tissue tumors, especially from myxoid liposarcoma, a malignancy that classically affects older individuals and shows pleomorphism, atypical lipoblasts and chromosome-12 translocation. A lipoblastoma diagnosis must be established only after careful consideration of all available clinical, radiologic, cytogenetic and morphologic data.
Asunto(s)
Lipoma/patología , Neoplasias de la Parótida/patología , Biopsia con Aguja , Niño , Humanos , Lipoma/diagnóstico , Lipoma/cirugía , Masculino , Neoplasias de la Parótida/diagnóstico , Neoplasias de la Parótida/cirugíaRESUMEN
This article presents a case of a young, otherwise asymptomatic male patient with a parotid gland enlargement. The initial clinical history did not reveal any risk factors related with HIV infection. A fine needle aspiration biopsy of the lesion showed a benign cystic lymphoepithelial lesion of the parotid gland. This once unusual lesion of the salivary gland has been recently associated with infection by the human immunodeficiency virus (HIV) and is presently encountered with increased frequency in the clinical practice. The knowledge of the association between these two entities led, in this case, to the diagnosis of HIV infection in an otherwise asymptomatic patient. Early detection of HIV infection is of vital importance since it has been demonstrated that prompt treatment of these patients with AZT slows down the progression of the disease
Asunto(s)
Enfermedades de las Parótidas/diagnóstico , Linfocele/diagnóstico , Síndrome de Inmunodeficiencia Adquirida/diagnóstico , Biopsia con Aguja , Enfermedades de las Parótidas/complicaciones , Enfermedades de las Parótidas/patología , Glándula Parótida/patología , Glándula Parótida , Linfocele/complicaciones , Linfocele/patología , Síndrome de Inmunodeficiencia Adquirida/complicaciones , Síndrome de Inmunodeficiencia Adquirida/patología , Tomografía Computarizada por Rayos XRESUMEN
La biopsia por aspiración con aguja fina esta actualmente aceptada como una técnica diagnóstica segura y confiable. En los pacientes que se presentan con enfermedad metastática diseminada de origin desconocido puede jugar un papel importante aportando un diagnóstico certero y rápido. Brindando de esta forma la oportundad de iniciar un plan terapéutico rápidamente. Esta técnica usualmente se puede realizar sin necesidad de hospitalizar al paciente con lo cual se logra reducir los costos tanto para el paciente como para el hospital. En los casos en que se llega a un diagnóstico definitivo se logra también evitarle una cirugía innecesaria al paciente. Este artículo presenta varios casos ilustrativos en los que se llegó a un diagnóstico final mediante el uso de la biopsia por aspiración con aguja fina