Perret Raul E, Josselin Nicolas, Knol Anne-Chantal, Khammari Amir, Cassecuel Julie, Peuvrel Lucie, Dreno Brigitte
Oncodermatology department, CIC, CHU, Nantes, France.
Histopathology Institute, Nantes, France.
Int J Dermatol. 2017 May;56(5):527-533. doi: 10.1111/ijd.13540. Epub 2017 Feb 10.
Immune checkpoint blockade therapy (ICBT) for the treatment of melanoma has led to an important improvement of overall survival in advanced stage patients. However, secondary cutaneous maculopapular eruptions (CMPEs) are frequent and remain poorly characterized.
We performed a retrospective analysis of melanoma patients from our institution who developed CMPEs during ICBT. Clinical information was retrieved, and histopathological and immunohistochemical characterization was performed by two pathologists. For comparison, a group of biopsies from CMPE caused by anti-v-raf murine sarcoma viral oncogene homolog B1 (BRAF) therapy was analyzed.
Eleven patients met the inclusion criteria. On clinical grounds, CMPE developed mainly on early onset of immunotherapy and were of low grade. Typical lesions included erythematous papules and macules affecting the trunk and/or extremities with associated pruritus. The histopathological patterns consisted of a superficial perivascular lymphocytic dermatitis (SPLD) with eosinophils followed by a granulomatous dermatitis. Other patterns included lichenoid, spongiotic, and a case of Grover's disease. The inflammatory infiltrate consisted of T lymphocytes (CD3 ) with a predominance of CD4 over CD8 cells; isolated Foxp3 cells were invariably present, and PD-1 was not expressed. Biopsies from CMPE caused by anti-BRAF therapy showed an SPLD and a similar lymphocytic immunophenotype.
Our study showed the clinical features of a group of melanoma patients with CMPE for ICBT and emphasized the wide spectrum of histological findings as well as their immunohistochemical profile. Differential diagnosis can be difficult with CMPE provoked by other therapies as was seen in our comparison group of anti-BRAF-induced eruptions.
免疫检查点阻断疗法(ICBT)用于治疗黑色素瘤已使晚期患者的总生存率得到显著提高。然而,继发性皮肤斑丘疹疹(CMPEs)很常见,其特征仍不明确。
我们对本院接受ICBT期间发生CMPEs的黑色素瘤患者进行了回顾性分析。收集临床信息,并由两名病理学家进行组织病理学和免疫组织化学特征分析。为作比较,分析了一组由抗v-raf鼠肉瘤病毒癌基因同源物B1(BRAF)治疗引起的CMPE活检样本。
11名患者符合纳入标准。从临床来看,CMPE主要在免疫治疗早期出现,且程度较轻。典型病变包括影响躯干和/或四肢的红斑丘疹和斑疹,并伴有瘙痒。组织病理学模式包括伴有嗜酸性粒细胞的浅表血管周围淋巴细胞性皮炎(SPLD),随后是肉芽肿性皮炎。其他模式包括苔藓样、海绵状以及1例格罗弗病。炎症浸润由T淋巴细胞(CD3)组成,其中CD4细胞多于CD8细胞;始终存在孤立的Foxp3细胞,且不表达PD-1。抗BRAF治疗引起的CMPE活检样本显示为SPLD和类似的淋巴细胞免疫表型。
我们的研究显示了一组接受ICBT的黑色素瘤患者发生CMPE的临床特征,并强调了组织学发现的广泛范围及其免疫组织化学特征。正如在我们抗BRAF诱导皮疹的比较组中所见,与其他疗法引起的CMPE进行鉴别诊断可能会很困难。