Chambelland A, Koeppel M-C, Desmedt E, Fongue J, Buono J-P, Berbis P, Delaporte E
Service de dermatologie, hôpital Nord, Assistance publique-Hôpitaux de Marseille, chemin des Bourrely, 13015 Marseille, France.
Service de dermatologie, hôpital Nord, Assistance publique-Hôpitaux de Marseille, chemin des Bourrely, 13015 Marseille, France.
Ann Dermatol Venereol. 2019 Oct;146(10):646-654. doi: 10.1016/j.annder.2019.06.002. Epub 2019 Jul 28.
Sorafenib is a multikinase inhibitor used in the treatment of hepatocellular carcinoma, advanced renal cell carcinoma, and differentiated thyroid carcinoma. Cutaneous adverse events are numerous and occur frequently.
We present two cases of nodulocystic lesions associated with comedones in patients treated with sorafenib for hepatocellular carcinoma. In the first patient, a 64-year-old man, lesions appeared on the trunk one year after beginning sorafenib. Histopathological examination revealed a non-granulomatous, perivascular and perisudoral polymorphic cellular infiltrate associated with comedones and microcysts. These lesions progressed via inflammatory episodes interrupted by long periods of spontaneous remission without any specific treatment. In the second patient, a 53-year-old woman, a rash appeared on the buttocks three months after starting sorafenib and then spread to the lumbar region and thighs. Histopathological examination was consistent with granulomatous acne lesions. The initial treatment (oral tetracycline and zinc) given for 3 months proved ineffective. Patient follow-up over 3 years showed gradual regression without the appearance of any further lesions.
In the literature, several reports discuss acneiform rashes in patients treated with targeted therapy. In most cases, these lesions were papulopustular without retentional lesions. There are few reports of nodulocystic eruptions associated with comedones following sorafenib therapy. The mechanisms of emergence of these lesions seem to involve inhibition of the RAF pathway, C-KIT, and the PDGF signaling pathway.
索拉非尼是一种多激酶抑制剂,用于治疗肝细胞癌、晚期肾细胞癌和分化型甲状腺癌。皮肤不良事件众多且频繁发生。
我们报告了两例在接受索拉非尼治疗肝细胞癌的患者中出现的伴有粉刺的结节囊肿性病变。第一例患者为一名64岁男性,在开始使用索拉非尼一年后,躯干出现病变。组织病理学检查显示为非肉芽肿性、血管周围和汗腺周围多形性细胞浸润,伴有粉刺和微囊肿。这些病变通过炎症发作进展,其间有长时间的自发缓解期,未进行任何特殊治疗。第二例患者为一名53岁女性,在开始使用索拉非尼三个月后,臀部出现皮疹,随后蔓延至腰部和大腿。组织病理学检查与肉芽肿性痤疮病变一致。最初给予的3个月口服四环素和锌治疗无效。对该患者进行了3年的随访,发现皮疹逐渐消退,未出现任何新的病变。
在文献中,有几篇报道讨论了接受靶向治疗患者的痤疮样皮疹。在大多数情况下,这些病变为丘疹脓疱性,无潴留性病变。关于索拉非尼治疗后出现伴有粉刺的结节囊肿性皮疹的报道很少。这些病变出现的机制似乎涉及RAF通路、C-KIT和血小板衍生生长因子信号通路的抑制。