Sawers A H, Davson J, Braganza J, Geary C G
J Clin Pathol. 1982 Jun;35(6):617-9. doi: 10.1136/jcp.35.6.617.
A case of systemic mastocytosis is described in which the finding on initial presentation was hepatosplenomegaly. No dermatological abnormality was present, and the bone marrow histology originally caused some confusion with primary myelofibrosis. The clinical course and the importance of distinguishing between these two diseases is discussed. The dermatological manifestation of systemic mastocytosis, in the form of urticaria pigmentosa, is well recognised, and alerts the physician to the underlying disease. In the absence of cutaneous signs, however, the diagnosis is less obvious. The case reported had predominantly marrow and splenic involvement by the disease process, giving rise to portal hypertension, and illustrates the problems of diagnosis which can arise.
本文描述了一例系统性肥大细胞增多症,其初诊表现为肝脾肿大。未发现皮肤异常,骨髓组织学最初与原发性骨髓纤维化有些混淆。文中讨论了这两种疾病的临床病程及鉴别诊断的重要性。系统性肥大细胞增多症的皮肤表现为色素性荨麻疹,这已广为人知,可提醒医生注意潜在疾病。然而,在没有皮肤体征的情况下,诊断就不那么明显了。报告的病例中,疾病过程主要累及骨髓和脾脏,导致门静脉高压,说明了可能出现的诊断问题。