Kaplan K J, Goodman Z D, Ishak K G
Department of Pathology, Walter Reed Army Medical Center, Washington, DC, USA.
Mod Pathol. 1999 Apr;12(4):370-8.
Nine cases of Langerhans' cell histiocytosis (LCH) of the liver are presented. Five of the patients had liver involvement only. Other organ systems, notably the lymph nodes and skin, were involved in the other four patients. Four of the patients had sclerosing biliary disease with infiltration of the bile ducts by Langerhans' cells, whereas in two other patients, the biliary sclerosis was not associated with direct hepatic involvement by Langerhans' cells. Histologically, the lesions were composed of focal aggregates of Langerhans' cells in a polymorphous background of mature eosinophils, lymphocytes, neutrophils, and plasma cells. LCH encompasses a syndrome that has a broad range of clinical presentations and that might involve the liver solely as tumor-like lesions or cystic lesions, or as part of systemic disease. Even when Langerhans' cells are not demonstrable, sclerosing cholangitis can be seen in LCH.
本文报告了9例肝脏朗格汉斯细胞组织细胞增多症(LCH)。其中5例患者仅肝脏受累。其他4例患者的其他器官系统,尤其是淋巴结和皮肤也受到累及。4例患者患有硬化性胆管疾病,朗格汉斯细胞浸润胆管,而另外2例患者的胆汁性硬化与朗格汉斯细胞直接累及肝脏无关。组织学上,病变由朗格汉斯细胞在成熟嗜酸性粒细胞、淋巴细胞、中性粒细胞和浆细胞组成的多形性背景中的局灶性聚集构成。LCH是一种具有广泛临床表现的综合征,可能仅以肿瘤样病变或囊性病变的形式累及肝脏,或作为全身疾病的一部分。即使朗格汉斯细胞无法被证实,在LCH中也可见硬化性胆管炎。