Reisberg I R, Oyakawa S
Am J Gastroenterol. 1987 Jan;82(1):54-60.
Mastocytosis is an unusual disorder of unknown etiology characterized by an abnormal proliferation of tissue mast cells. We present a case of a young woman with systemic mastocytosis with malabsorption secondary to small bowel invasion by mast cells, myelofibrosis, and massive exudative ascites secondary to mass cell invasion of the intraabdominal lymph nodes. The patient responded favorably to a combined therapy with histamine H1 and H2 receptor antagonists and corticosteroids. We include a review of the literature.
肥大细胞增多症是一种病因不明的罕见疾病,其特征为组织肥大细胞异常增殖。我们报告一例年轻女性系统性肥大细胞增多症病例,该患者因肥大细胞侵犯小肠继发吸收不良、骨髓纤维化,以及因肥大细胞侵犯腹腔淋巴结继发大量渗出性腹水。患者对组胺H1和H2受体拮抗剂及皮质类固醇的联合治疗反应良好。我们还纳入了文献综述。