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一名患有朗格汉斯细胞组织细胞增多症的婴儿脾脏和胰腺病变的超声表现。

The sonographic appearance of lesions of the spleen and pancreas in an infant with Langerhans' cell histiocytosis.

作者信息

Muwakkit S, Gharagozloo A, Souid A K, Spirt B A

机构信息

Department of Pediatrics, SUNY Health Science Center, Syracuse 13210.

出版信息

Pediatr Radiol. 1994;24(3):222-3. doi: 10.1007/BF02012200.

Abstract

Langerhans' cell histiocytosis (LCH), the term now used to describe the group of diseases known as histiocytosis X, is a rare disorder of the bone marrow-derived histiocytes that may involve the skin, bone, bone marrow, liver, spleen, lungs, lymph nodes, and rarely the pancreas. Sonographically demonstrable lesions of the spleen and pancreas have not been reported. We present a case of disseminated LCH in a 4-week-old infant to demonstrate the sonographic appearance of splenic and pancreatic lesions that occur with this disease.

摘要

朗格汉斯细胞组织细胞增多症(LCH),该术语现用于描述一组曾被称为组织细胞增多症X的疾病,是一种源自骨髓的组织细胞的罕见病症,可能累及皮肤、骨骼、骨髓、肝脏、脾脏、肺、淋巴结,很少累及胰腺。超声可显示的脾脏和胰腺病变尚未见报道。我们报告一例4周龄婴儿播散性LCH病例,以展示该病出现时脾脏和胰腺病变的超声表现。

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