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Bilateral giant parathyroid adenoma and hungry bone syndrome: a case report.
Martínez-Loya, Carolina; Granados-Gutiérrez, Dalai E; Torrens-Chacón, Anagabriela; Rodríguez-Luna, David A; Frayre-García, Zabdy E; Villegas-Vázquez, Leonela; Enríquez-Sánchez, Luis B.
Afiliação
  • Martínez-Loya C; Departamento de Investigación, Universidad Autonóma de Chihuahua, Facultad de Medicina y Ciencias Biomédicas, Nuevo Campus Universitario, 31125, Chihuahua, Mexico. caromtzloy@icloud.com.
  • Granados-Gutiérrez DE; Departamento de Cirugía, Hospital Central del Estado, Antonio Rosales 33000, Obrera, 31350, Chihuahua, Mexico.
  • Torrens-Chacón A; Departamento de Cirugía, Hospital Central del Estado, Antonio Rosales 33000, Obrera, 31350, Chihuahua, Mexico.
  • Rodríguez-Luna DA; Departamento de Medicina Interna, Hospital Central del Estado, Antonio Rosales 33000, Obrera, 31350, Chihuahua, Mexico.
  • Frayre-García ZE; Departamento de Medicina Interna, Hospital Central del Estado, Antonio Rosales 33000, Obrera, 31350, Chihuahua, Mexico.
  • Villegas-Vázquez L; Médico Interno de Pregrado, Hospital Central del Estado, Antonio Rosales 33000, Obrera, 31350, Chihuahua, Mexico.
  • Enríquez-Sánchez LB; Departamento de Investigación, Universidad Autonóma de Chihuahua, Facultad de Medicina y Ciencias Biomédicas, Nuevo Campus Universitario, 31125, Chihuahua, Mexico.
J Med Case Rep ; 17(1): 373, 2023 Sep 01.
Article em En | MEDLINE | ID: mdl-37653552
BACKGROUND: There is some evidence supporting the idea that double parathyroid adenomas represent a different entity from multiglandular hyperplasia; however, the distinction among them is not straightforward. CASE PRESENTATION: We described a case of primary hyperparathyroidism (PHPT) with pronounced clinical manifestations, caused by a bilateral giant parathyroid adenoma. A 34-year-old Hispanic/Latino male was diagnosed with PHPT caused by two giant parathyroid adenomas. The preoperative tests were neck ultrasound and computed tomography scan (CT-scan), showing two masses in the territory of parathyroid glands, bilaterally distributed (right was 31 × 18 × 19 mm and the left was 38 × 15 × 14 mm); sestamibi scan was not available. Parathyroid hormone (PTH) was highly elevated. Multiple complications of PHPT were present, such as bone lytic lesions, renal and pancreatic calcifications, and cardiovascular disease, the latter of which is an overlooked complication of PHPT. Multiple endocrine neoplasia 1 and 2 (MEN 1/2) were ruled out by the absence of clinical, biochemical, and radiological findings in other endocrine glands. The patient underwent subtotal parathyroidectomy with an intraoperative histopathological study; both intraoperative and definitive histopathology results were consistent with parathyroid adenomas; afterward, adequate suppression of PTH was assured, and later on, the patient presented hungry bone syndrome (HBS). CONCLUSIONS: The diagnosis of double parathyroid adenomas is difficult. Regarding the similarities between multiglandular hyperplasia and parathyroid adenomas, this case report contributes to the further distinction between these two clinical entities. This case report also represents, in particular, the challenge of difficult diagnosis in places with limited resources, such as developing countries.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Paratireoides / Doenças Ósseas / Hipocalcemia Limite: Adult / Humans Idioma: En Revista: J Med Case Rep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Paratireoides / Doenças Ósseas / Hipocalcemia Limite: Adult / Humans Idioma: En Revista: J Med Case Rep Ano de publicação: 2023 Tipo de documento: Article País de afiliação: México País de publicação: Reino Unido