Chen K R, Tanaka M, Miyakawa S
Division of Dermatology, Ogikubo Hospital, Tokyo, Japan.
Br J Dermatol. 1998 Mar;138(3):522-5. doi: 10.1046/j.1365-2133.1998.02138.x.
We report a case of granulomatous mycosis fungoides that progressed into fatal gastrointestinal involvement 4 years after the onset of skin lesions, despite improvement of the skin lesions in response to a combination of PUVA and systemic interferon-gamma therapy. Histological examination showed Pautrier's microabscesses with granuloma annulare-like features and sarcoidal granuloma formation in the plaque stage, proliferation of blast-transformed atypical lymphocytes with persistent granuloma formation in the tumour stage, and metastatic lesions. A literature review of granulomatous mycosis fungoides revealed that 11 of the 24 reported cases died of the disease, and like our case, seven died within 5 years. We suggest that mycosis fungoides with granulomatous reactions does not indicate a favourable prognosis.
我们报告一例肉芽肿性蕈样霉菌病,尽管皮肤病变在补骨脂素紫外线A(PUVA)和全身干扰素-γ治疗联合应用后有所改善,但在皮肤病变出现4年后进展为致命的胃肠道受累。组织学检查显示,斑块期有呈环状肉芽肿样特征的帕特里尔微脓肿和结节病样肉芽肿形成,肿瘤期有母细胞转化的非典型淋巴细胞增殖并持续存在肉芽肿形成,以及转移病灶。对肉芽肿性蕈样霉菌病的文献综述显示,24例报告病例中有11例死于该病,与我们的病例一样,7例在5年内死亡。我们认为,伴有肉芽肿反应的蕈样霉菌病并不预示预后良好。