Callot V, Roujeau J C, Bagot M, Wechsler J, Chosidow O, Souteyrand P, Morel P, Dubertret L, Avril M F, Revuz J
Department of Dermatology, Hôpital Henri Mondor, Creteil, France.
Arch Dermatol. 1996 Nov;132(11):1315-21.
To test the hypothesis that drug-induced pseudolymphoma and hypersensitivity syndrome are 2 distinct clinical entities.
Retrospective study from 1980 to 1993.
Departments of dermatology and medicine of 5 referral universitary hospitals.
Twenty-four patients who met arbitrary criteria selected as being suggestive of lymphoma, with probable drug cause. Patients with other definite cutaneous drug-induced eruptions were excluded.
None.
Suspect drugs; clinical, biological, and pathological findings; and evolution of each case and of 110 published case reports.
Two groups were separated according to their mode of onset and clinical aspect. Three patients (and 15 cases in the literature) had subacute papulonodular or infiltrated plaques, without visceral involvement. Skin biopsy specimens showed a dense lymphocytic infiltrate mimicking lymphoma. Healing was constant when the drug was stopped. The 21 remaining patients (and 95 published cases) had an acute widespread eruption, with fever, enlarged lymph nodes, and multivisceral involvement. Lymphocytosis, atypical lymphocytes, eosinophilia, hepatitis, and high levels of lactate dehydrogenase were frequent. Skin biopsy findings were usually not specific (lymphocytic infiltrate and keratinocyte necrosis) but sometimes mimicked lymphoma. Severe forms and relapses occurred, even after the drug was stopped. The inducing drugs were the same in the 2 groups.
These 2 groups correspond to drug-induced pseudolymphoma and hypersensitivity syndrome. We think that they are 2 distinct entities with different clinical and biological features and outcome, even if the pathological findings are sometimes similar. Prospective studies are needed to confirm these facts, to evaluate the therapy, and to follow up patients.
检验药物性假性淋巴瘤和超敏反应综合征是两种不同临床实体的假说。
1980年至1993年的回顾性研究。
5家转诊大学医院的皮肤科和内科。
24名符合任意提示淋巴瘤标准且可能由药物引起的患者。排除有其他明确皮肤药物性皮疹的患者。
无。
可疑药物;临床、生物学和病理学发现;以及每个病例和110篇已发表病例报告的病情演变。
根据发病方式和临床表现将患者分为两组。3名患者(以及文献中的15例)有亚急性丘疹结节性或浸润性斑块,无内脏受累。皮肤活检标本显示密集淋巴细胞浸润,类似淋巴瘤。停药后病情持续好转。其余21名患者(以及95篇已发表病例)有急性全身性皮疹,伴有发热、淋巴结肿大和多脏器受累。淋巴细胞增多、非典型淋巴细胞、嗜酸性粒细胞增多、肝炎以及高乳酸脱氢酶水平很常见。皮肤活检结果通常不具特异性(淋巴细胞浸润和角质形成细胞坏死),但有时类似淋巴瘤。即使停药后仍会出现严重形式和复发。两组的诱发药物相同。
这两组分别对应药物性假性淋巴瘤和超敏反应综合征。我们认为它们是两种不同的实体,具有不同的临床、生物学特征和预后,即使病理结果有时相似。需要进行前瞻性研究以证实这些事实、评估治疗方法并对患者进行随访。