Mwasakyalo Gideon Safiel, Bright Frank, Mbwambo Orgenes Jasper, Ngowi Bartholomeo Nicholaus, Mwakibibi Daniel, Mbwambo Jasper Saidi, Majura Musa Raymond, Sanga Evans Azina, Mremi Alex
Department of Urology Kilimanjaro Christian Medical Centre Moshi Tanzania.
Faculty of Medicine Kilimanjaro Christian Medical University College Moshi Tanzania.
Clin Case Rep. 2024 Mar 8;12(3):e8659. doi: 10.1002/ccr3.8659. eCollection 2024 Mar.
The mainstays of treatment for granuloma pyogenicum include careful evaluation of any penile growth, thorough excision of the polypoid, histological examination, and close monitoring to check relapse and management.
Pyogenic granuloma is an acquired noncancerous vascular proliferation that arises from the mucosa and skin, seldom subcutaneously or intravascularly. It is also referred to as telangiectasis granuloma or lobular capillary haemangioma. The risk factors include vascular abnormalities, medicines, hormones, and microtrauma. We discussed the case of a 24-year-old man who had a poorly managed ventral distal penile polypoid lesion at a peripheral hospital. Upon further histopathological examination, the diagnosis of pyogenic granuloma was made. Histopathologically speaking, the term "pyogenic granuloma" is misleading because the illness is not linked to the production of granulomas. Pyogenic granuloma's etiopathogenesis is still unknown; true hemangioma is thought to be a reactive hyperproliferative of the vasculature brought on by a variety of stimuli; pyogenic granuloma may be caused by uneven angiogenic factor production in response to minor local trauma or cutaneous disease. Histopathological analysis and surgical excision are the methods used for diagnosis and treatment. The mainstay of treatment for granuloma pyogenic granuloma includes careful evaluation of any penile growth, thorough excision of the polypoid, histological examination, close follow-up to check for relapse, and early management.
脓性肉芽肿的主要治疗方法包括对任何阴茎肿物进行仔细评估、彻底切除息肉样肿物、组织学检查以及密切监测以检查复发情况并进行处理。
脓性肉芽肿是一种后天性非癌性血管增生,起源于黏膜和皮肤,很少发生于皮下或血管内。它也被称为毛细血管扩张性肉芽肿或小叶性毛细血管瘤。危险因素包括血管异常、药物、激素和微创伤。我们讨论了一名24岁男性的病例,他在外院对阴茎腹侧远端息肉样病变处理不当。经进一步组织病理学检查,诊断为脓性肉芽肿。从组织病理学角度来说,“脓性肉芽肿”这个术语具有误导性,因为该病与肉芽肿的形成并无关联。脓性肉芽肿的发病机制仍不清楚;真正的血管瘤被认为是由多种刺激引起的血管反应性过度增生;脓性肉芽肿可能是由于对轻微局部创伤或皮肤疾病的血管生成因子产生不均衡所致。组织病理学分析和手术切除是用于诊断和治疗的方法。脓性肉芽肿的主要治疗方法包括对任何阴茎肿物进行仔细评估、彻底切除息肉样肿物、组织学检查、密切随访以检查复发情况以及早期处理。