Ferguson Nkanyezi N, Asarch Adam, VanBeek Marta, Swick Brian L
Department of Dermatology, University of Iowa Hospital and Clinics, Iowa City, IA 52242, USA.
Am J Dermatopathol. 2013 Jun;35(4):e63-6. doi: 10.1097/DAD.0b013e31827b7674.
Acute mucocutaneous methotrexate toxicity is not classically associated with prominent tissue eosinophilia. We present a case of acute methotrexate toxicity associated with pancytopenia and mucocutaneous erosion with interface dermatitis and numerous eosinophils. A 79-year-old male, with a history of psoriasis vulgaris on methotrexate therapy, presented with blisters of the oral mucosa, groin, sacrum, and extremities after daily consumption of methotrexate. Examination revealed blisters and erosions localized to psoriatic plaques, the perineum, and the oral mucosa. Laboratory evaluation demonstrated pancytopenia, megaloblastic anemia, and elevated liver function tests. A skin biopsy of an eroded plaque revealed psoriasiform epidermal hyperplasia with epidermal erosion, parakeratosis, and loss of the granular cell layer. There was an underlying band-like lymphoid infiltrate with interface dermatitis, dyskeratotic keratinocytes, and numerous eosinophils. Direct immunofluorescence studies were negative for the deposition of immunoreactants. Methotrexate was held, and the patient received leucovorin resulting in improvement of blood counts and cutaneous lesions. The histopathologic changes associated with acute mucocutaneous toxicity have been described as pauci-inflammatory erosions associated with dyskeratotic keratinocytes to interface dermatitis with necrotic keratinocytes and occasionally associated eosinophils. Although these changes are most often superimposed on psoriatic plaques, they have been reported to occur on normal skin. Therefore, the differential diagnosis may include lichen planus, a lichenoid drug eruption, or a fixed drug eruption, and given the presence of mucosal ulceration, incipient pemphigus vulgaris or paraneoplastic pemphigus vulgaris. This case illustrates that acute mucocutaneous methotrexate toxicity may be associated with both interface dermatitis and numerous eosinophils.
急性皮肤黏膜甲氨蝶呤毒性通常与显著的组织嗜酸性粒细胞增多无关。我们报告一例急性甲氨蝶呤毒性病例,该病例伴有全血细胞减少、皮肤黏膜糜烂,伴有界面性皮炎和大量嗜酸性粒细胞。一名79岁男性,有寻常型银屑病病史,正在接受甲氨蝶呤治疗,在每日服用甲氨蝶呤后,出现口腔黏膜、腹股沟、骶部和四肢水疱。检查发现水疱和糜烂局限于银屑病斑块、会阴和口腔黏膜。实验室检查显示全血细胞减少、巨幼细胞贫血和肝功能检查升高。对一处糜烂斑块进行皮肤活检,显示银屑病样表皮增生,伴有表皮糜烂、角化不全和颗粒细胞层缺失。有潜在的带状淋巴细胞浸润,伴有界面性皮炎、角化不良的角质形成细胞和大量嗜酸性粒细胞。直接免疫荧光研究显示免疫反应物沉积为阴性。停用甲氨蝶呤,患者接受亚叶酸钙治疗,导致血细胞计数和皮肤病变改善。与急性皮肤黏膜毒性相关的组织病理学变化被描述为与角化不良的角质形成细胞相关的少炎症性糜烂,至伴有坏死角质形成细胞且偶尔伴有嗜酸性粒细胞的界面性皮炎。尽管这些变化最常叠加在银屑病斑块上,但据报道也可发生在正常皮肤上。因此,鉴别诊断可能包括扁平苔藓、苔藓样药疹或固定性药疹,鉴于存在黏膜溃疡,还可能包括早期寻常型天疱疮或副肿瘤性天疱疮。本病例说明急性皮肤黏膜甲氨蝶呤毒性可能与界面性皮炎和大量嗜酸性粒细胞有关。