Sarwate Mrinal, Bakhshwin Ahmed
Robert Tomisch Pathology and Laboratory Medicine Institute, Cleveland Clinic, Cleveland, OH.
King Abdulaziz University, Jeddah, Saudi Arabia.
ACG Case Rep J. 2023 Jul 7;10(7):e01089. doi: 10.14309/crj.0000000000001089. eCollection 2023 Jul.
Systemic mastocytosis is a rare myeloproliferative disorder characterized by abnormal accumulation of mast cells in a variety of organs. When affecting the gastrointestinal tracts, it may manifest with steatorrhea, malabsorption, hepatomegaly, splenomegaly, portal hypertension, and ascites, among others. To our knowledge, only one case of systemic mastocytosis has been reported affecting the appendix. We present another case of a 47-year-old woman who was admitted for right-sided acute abdominal pain and found to have systemic mastocytosis in her appendectomy specimen as the first and only manifestation of her disease.
系统性肥大细胞增多症是一种罕见的骨髓增殖性疾病,其特征是肥大细胞在多种器官中异常积聚。当累及胃肠道时,可能表现为脂肪泻、吸收不良、肝肿大、脾肿大、门静脉高压和腹水等。据我们所知,仅有一例系统性肥大细胞增多症累及阑尾的报道。我们现报告另一例47岁女性患者,她因右侧急性腹痛入院,在阑尾切除标本中发现系统性肥大细胞增多症,这是其疾病的首发且唯一表现。