Raina V, Young P T, Foulis A K, Soukop M
Department of Medical Oncology, Royal Infirmary, Glasgow, UK.
Postgrad Med J. 1989 Feb;65(760):83-5. doi: 10.1136/pgmj.65.760.83.
A 58 year old woman, with dermatitis herpetiformis was found to have Hodgkin's disease following the discovery of an abdominal mass and splenomegaly. Combination chemotherapy was given. Although the abdominal mass and systemic symptoms resolved, the splenomegaly did not and the patient developed severe prolonged anaemia and pancytopaenia. Splenectomy resulted in a complete reversal of the haematological abnormalities. Histopathological examination of the spleen revealed fungal granulomas of Candida albicans. No residual Hodgkin's disease was found. The patient thus had hypersplenism due to fungal granulomas in the spleen. This form of presentation of fungal granuloma is very rare and resulted in delay in diagnosis and considerable morbidity to the patient.
一名58岁患有疱疹样皮炎的女性,在发现腹部肿块和脾肿大后被诊断出患有霍奇金病。给予联合化疗。尽管腹部肿块和全身症状得到缓解,但脾肿大并未改善,患者出现了严重且持续时间较长的贫血和全血细胞减少。脾切除术后血液学异常完全逆转。脾脏的组织病理学检查显示白色念珠菌真菌肉芽肿。未发现残留的霍奇金病。因此,该患者因脾脏真菌肉芽肿导致脾功能亢进。这种真菌肉芽肿的表现形式非常罕见,导致了诊断延迟和患者相当大的发病率。