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1.
Korean Journal of Medicine ; : 179-184, 2016.
Artigo em Coreano | WPRIM | ID: wpr-101519

RESUMO

Some patients have ascites without having liver disease, so it is important to analyze the cause of these ascites. Tuberculous peritonitis is an infectious disease characterized by lymphocyte-dominant exudative ascites. In contrast, myxedema ascites is a very rare disease characterized by a high serum/ascites albumin gradient (SAAG) with hypothyroidism. We herein report a case involving a 48-year-old woman with both diseases simultaneously. She was hospitalized because of massive ascites, generalized edema, and a puffy face. Hypothyroidism was confirmed by thyroid function tests. Her ascitic fluid had a high SAAG; no other specific findings were identified by cytology, culture, or computed tomography. Three months after initiating drug therapy for the hypothyroidism, the patient's systemic edema improved but the ascites recurred. Accordingly, diagnostic laparoscopy was performed, and tuberculous peritonitis was confirmed. As seen in this case, when myxedema ascites is associated with tuberculous peritonitis, an accurate diagnosis may be challenging.


Assuntos
Feminino , Humanos , Pessoa de Meia-Idade , Ascite , Líquido Ascítico , Doenças Transmissíveis , Diagnóstico , Tratamento Farmacológico , Edema , Hipotireoidismo , Laparoscopia , Hepatopatias , Mixedema , Peritonite Tuberculosa , Doenças Raras , Testes de Função Tireóidea
2.
Journal of Liver Cancer ; : 139-144, 2016.
Artigo em Coreano | WPRIM | ID: wpr-76007

RESUMO

Sarcomatoid carcinoma arising from intrahepatic cholangiocyte, an extremely rare primary liver cancer, has highly invasive and metastatic potential. The pathogenesis of this tumor is unclear, although histogenetic mechanisms, such as transdifferentiation/dedifferentiation (epithelial-mesenchymal transition or metaplastic transformation), biphasic differentiation (combination and collision), and redifferentiation, might be suggested to explain the simultaneous co-existence of carcinoma and sarcoma components in the same tumor. Immunohistochemical staining might be necessary to differentiate whether sarcomatous component is originated from hepatocyte or cholangiocyte. We report a case of sarcomatoid intrahepatic cholangiocarcinoma in a 58 year-old man presenting as an incidentally detected liver mass on regular health examination, which was diagnosed by an application of immunohistochemical methods after surgical resection, with a review of the literature based on 9 cases reported in Korea.


Assuntos
Colangiocarcinoma , Hepatócitos , Coreia (Geográfico) , Neoplasias Hepáticas , Fígado , Sarcoma
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