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一例表现为肝硬变样的侵袭性系统性肥大细胞增生症罕见病例。

An unusual case of aggressive systemic mastocytosis mimicking hepatic cirrhosis.

机构信息

1 Department of Pathology, Second Hospital of Tianjin Medical University, Tianjin 300211, China ; 2 Department of Dermatology, Traditional Chinese Medical Hospital of Rizhao, Rizhao 276000, China.

出版信息

Cancer Biol Med. 2014 Jun;11(2):134-8. doi: 10.7497/j.issn.2095-3941.2014.02.009.

Abstract

Hepatic involvement in aggressive systemic mastocytosis (ASM) is relatively common, and the main clinical features of this disease include hepatomegaly, portal hypertension, ascites, and fibrosis. Cirrhosis is a rare ASM symptom. We report an ASM case that initially mimicked cirrhosis based on clinical and radiographic analyses. The portal tract was expanded by mononuclear inflammatory cells, and an increase in collagen amount was observed in routine histological sections of the biopsied liver. A diagnosis of systemic mastocytosis (SM) was made after ancillary tests for mast cells using bone marrow aspirates. Extensive involvement of the liver and gastrointestinal tract was observed. Clinicians and pathologists need to consider ASM as a diagnosis or differential diagnosis in a clinical case of cirrhosis with unknown etiology. The diagnosis can be confirmed or disregarded by immunohistochemical staining and molecular analysis.

摘要

肝受累在侵袭性系统性肥大细胞增多症(ASM)中较为常见,其主要临床特征包括肝肿大、门静脉高压、腹水和纤维化。肝硬化是 ASM 的罕见症状。我们报告了一例最初基于临床和影像学分析而类似于肝硬化的 ASM 病例。门管区被单核炎性细胞扩张,活检肝脏的常规组织学切片中观察到胶原量增加。骨髓抽吸术用于肥大细胞的辅助检查后,诊断为系统性肥大细胞增多症(SM)。广泛累及肝脏和胃肠道。临床医生和病理学家需要考虑在病因不明的肝硬化临床病例中,将 ASM 作为诊断或鉴别诊断。通过免疫组织化学染色和分子分析可确认或排除诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c6e/4069804/bf1a93d9c325/cbm-11-02-134-f1.jpg

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