McCarty Thomas R, Hung Adelina, Mohanty Arpan, Allen John I
Department of Internal Medicine, Yale University School of Medicine, New Haven, CT.
Section of Digestive Diseases, Yale University School of Medicine, New Haven, CT.
ACG Case Rep J. 2017 Mar 1;4:e30. doi: 10.14309/crj.2017.30. eCollection 2017.
Systemic mastocytosis is a myeloproliferative disorder characterized by extracutaneous involvement of at least one organ. Although rare, infiltration of inflammatory mast cells within the portal vein may lead to obstruction of the sinusoids resulting in non-cirrhotic portal hypertension. We present a patient with known history of systemic mastocytosis with bone marrow involvement presenting with new-onset esophageal variceal bleeding. Although systemic mastocytosis is uncommon, the subsequent development of hepatic involvement and non-cirrhotic portal hypertension are discussed. Further highlighted is a lack of organization guidelines and the potential for gastrointestinal and hepatic screening of mastocytosis patients with known extracutaneous involvement.
系统性肥大细胞增多症是一种骨髓增殖性疾病,其特征是至少一个器官有皮肤外受累。虽然罕见,但炎症性肥大细胞浸润门静脉可导致肝血窦阻塞,从而引起非肝硬化性门静脉高压。我们报告一名有系统性肥大细胞增多症病史且骨髓受累的患者,该患者出现了新发的食管静脉曲张出血。虽然系统性肥大细胞增多症并不常见,但本文讨论了随后发生的肝脏受累及非肝硬化性门静脉高压。本文还进一步强调了缺乏组织指南以及对已知有皮肤外受累的肥大细胞增多症患者进行胃肠道和肝脏筛查的可能性。