Cohen Philip R, Schulze Keith E, Tschen Jaime A, Hetherington George W, Nelson Bruce R
Dermatologic Surgery Center of Houston, Houston, TX, USA.
South Med J. 2006 Apr;99(4):396-402. doi: 10.1097/01.smj.0000209223.68763.b1.
Extramammary Paget disease is an uncommon cutaneous neoplasm that presents as erythematous plaques most frequently located in the anogenital region. Management of patients with extramammary Paget disease involves evaluation of the individual for: (1) a disease-associated, unsuspected, visceral malignancy and (2) secondary adenocarcinoma in the underlying dermis or regional lymph nodes. Several modalities, each with variable effectiveness, are available to treat the cutaneous component of the disease: electrodesiccation and curettage, laser surgery, aminolevulinic acid photodynamic therapy, radiotherapy, topical chemotherapy, and wide surgical excision. However, surgical excision using the Mohs micrographic technique is currently the modality of choice for treating the cutaneous lesions of extramammary Paget disease. Recently, a topical imidazoquinoline immunomodulator that induces cytokine production and stimulates the innate and cellular immune responses--imiquimod cream-has been used for the management of primary or relapsing extramammary Paget disease. Complete healing, without recurrence, of extramammary Paget disease in patients whose cutaneous lesions were treated topically with imiquimod 5% cream was observed. We describe a man with suprapubic extramammary Paget disease whose condition was primary and limited to his skin. Biopsy-confirmed complete resolution of his disease was observed after the topical application of imiquimod 5% cream 3 times per week (on alternate days) for 16 weeks. After reviewing the published reports of other patients with extramammary Paget disease whose disease was successfully treated with imiquimod cream, we suggest that topical imiquimod 5% cream-at least 3 times per week (with 1-2 d of nontreatment in between) for a minimum of 8 to 16 weeks--be considered as an initial treatment for primary cutaneous extramammary Paget disease. Surgical excision or an alternative therapeutic modality is recommended for patients whose extramammary Paget disease persists or recurs after treatment with topical imiquimod.
乳房外佩吉特病是一种罕见的皮肤肿瘤,表现为最常位于肛门生殖器区域的红斑性斑块。乳房外佩吉特病患者的管理包括对个体进行评估,以确定:(1)与疾病相关的、未被怀疑的内脏恶性肿瘤,以及(2)潜在真皮层或区域淋巴结中的继发性腺癌。有几种治疗该疾病皮肤成分的方法,每种方法的有效性各不相同:电干燥刮除术、激光手术、氨基乙酰丙酸光动力疗法、放射疗法、局部化疗和广泛手术切除。然而,目前使用莫氏显微描记手术技术进行手术切除是治疗乳房外佩吉特病皮肤病变的首选方法。最近,一种能诱导细胞因子产生并刺激先天性和细胞免疫反应的局部咪唑喹啉免疫调节剂——咪喹莫特乳膏,已被用于治疗原发性或复发性乳房外佩吉特病。观察到用5%咪喹莫特乳膏局部治疗皮肤病变的乳房外佩吉特病患者实现了完全愈合且无复发。我们描述了一名患有耻骨上乳房外佩吉特病的男性,其病情为原发性且仅限于皮肤。在每周3次(隔日)局部应用5%咪喹莫特乳膏16周后,活检证实其疾病完全消退。在回顾了其他使用咪喹莫特乳膏成功治疗乳房外佩吉特病患者的已发表报告后,我们建议将局部应用5%咪喹莫特乳膏——每周至少3次(中间间隔1 - 2天不治疗),持续至少8至16周——视为原发性皮肤乳房外佩吉特病的初始治疗方法。对于乳房外佩吉特病在用局部咪喹莫特治疗后持续存在或复发的患者,建议进行手术切除或采用替代治疗方法。