Sarnoff D S, DeFeo C P
Arch Dermatol. 1985 May;121(5):669-72.
Mycosis fungoides was documented in a patient two years after pemphigus foliaceus had been diagnosed and treated with corticosteroids. Eight years later, the patient was found to have stage IV lymphomatous disease with generalized erythroderma and palpable, histologically positive lymph nodes. Hematoxylin-eosin staining of a specimen of erythroderma revealed mycosis fungoides, while direct immunofluorescence of this tissue revealed intercellular IgG deposits diagnostic of pemphigus foliaceus.
在一名患者被诊断为落叶型天疱疮并用皮质类固醇治疗两年后,记录到蕈样肉芽肿。八年后,该患者被发现患有IV期淋巴瘤疾病,伴有全身性红皮病和可触及的、组织学检查呈阳性的淋巴结。红皮病标本的苏木精-伊红染色显示为蕈样肉芽肿,而该组织的直接免疫荧光显示细胞间IgG沉积,可诊断为落叶型天疱疮。