背景:迄今为止,只有有限数量的病例报告记录了医学文献中PNS和黑素细胞痣的同时发生.这项研究旨在报告一例罕见的后胸壁PNS与黑素细胞痣结合的病例。
方法:一名46岁女性,在她的左上后胸壁上有一个长期的黑色病变,在演讲前的两个月里,这变得很痛苦。有一个痛苦,深蓝色,非红斑,左上后胸壁无触痛结节。基于患者对美容目的的渴望,在局部麻醉下,将病灶完全切除,初次闭合。组织病理学检查显示皮内黑素细胞痣伴毛发窦发炎。
结论:与痣相关的后胸壁PNS的稀有性对临床医生提出了独特的诊断和治疗挑战。独特的解剖位置,不同于传统地区,而这两种情况之间的罕见关联可能会延迟准确诊断,并导致管理不善或干预不当.
结论:后胸壁PNS是另一种非常罕见的非典型PNS。PNS和蓝痣之间的关联是一个令人着迷的医学发现,值得进一步研究。
BACKGROUND: To date, only a limited number of case reports have documented the co-occurrence of PNS and melanocytic
nevus in the medical literature. This study aims to report an exceptionally rare case of posterior chest wall PNS in conjunction with a melanocytic
nevus.
METHODS: A 46-year-old female presented with a long-standing black lesion on her left upper posterior chest wall, that had become painful in the two months prior to presentation. There was a painful, dark blue, non-erythematous, and non-tender nodule on the left upper posterior chest wall. Based on the patient\'s desire for cosmetic purposes, the lesion was excised totally with primary closure under local anaesthesia. Histopathological examination revealed intradermal melanocytic
nevus with inflamed pilonidal sinus.
CONCLUSIONS: The rarity of posterior chest wall PNS associated with nevi poses unique diagnostic and therapeutic challenges for clinicians. The distinct anatomical location, different from the conventional region, and the rare association between the two conditions may delay accurate diagnosis and result in mismanagement or inappropriate interventions.
CONCLUSIONS: The posterior chest wall PNS is another type of atypical PNS that is extremely rare. The association between PNS and blue
nevus is a fascinating medical finding that deserves further investigation.