World journal of hepatology · 2013
A rare case of hyaline-type Castleman disease in the liver.
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Miyoshi Hisaaki, Mimura Shima, Nomura Takako, Tani Joji, Morishita Asahiro, Kobara Hideki, Mori Hirohito, Yoneyama Hirohito, Deguchi Akihiro, Himoto Takashi, Yamamoto Naoki, Okano Keiichi, Suzuki Yasuyuki, Masaki Tsutomu
Аннотация
Castleman disease often develops in the neck, mediastinum and pulmonary hilum. Its onset in the peritoneal cavity is very rare. The patient, a woman in her 70s, was referred to our department for a detailed examination of an abdominal mass. On abdominal ultrasonography, computed tomography scan, magnetic resonance imaging and positron emission tomography, a mass approximately 15 mm in diameter was noted in the hepatic S6. We attempted radical treatment and conducted a laparoscope-assisted right lobectomy. On the basis of histopathological findings, the patient was diagnosed as having hyaline type Castleman disease in the liver, a very rare condition.