Recurrent angiokeratoma scroti: a case report

S. Tomar, B. Thakur, K. Sankhala
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Epidermis revealed variable degree of acanthosis and elongation of rete ridges and mild hyperkeratosis. Electrocauterisation of lesions was done and the follow-up period of three months was uneventful. Conclusion Although angiokeratoma scroti is not an uncommon entity, good treatment modality with minimal adverse effects in terms of complete resolution of diffuse lesions, recurrence, scarring, crusting, bleeding or cosmetic results is still not available. Introduction The term angiokeratoma is used to describe several distinct entities characterised by vascular nodules in the skin, with a histological picture of dermal vascular ectasia surmounted by hyperkeratosis of the epidermis. Angiokeratoma of the scrotum was originally described by Fordyce in 18961 reporting a case of 60-year-old man with multiple warty lesions confined to the scrotum only. Only a few cases of recurrent angiokeratoma had been reported since then. We describe here an adult male presenting with multiple papules over the scrotum with a previous history of two recurrences. Case report A 34-year-old male presented in the surgery department with moderate itching and multiple papules arranged diffusely over the scrotum. There was history of two recurrences five and three years back with the same complaints. Electrocauterisation of lesions was previously done two times, although no previous pathological reports were available. Each time, the follow-up period of four to six months had been uneventful. Even after complete post-operative healing, the patient continued to experience persistent discomfort, pruritis and psychological distress. Mere contact of the affected area with his underwear resulted in constant irritation. There was no history of trauma, episodic bleeding, similar lesions somewhere else on his body, inguinal hernia, genitourinary tumours, thrombophlebitis or varicocele. Physical examination revealed multiple, soft, bluish-red, compressible papules of 3–4 mm diameter with excoriation marks and focal thickening of skin, which might be due to previous surgical intervention. Systemic examination and routine investigations including urine examination and ultrasonography of scrotum were unremarkable. This time also, lesions were electrocauterised and excised biopsy tissue, consisting of multiple greyish white pieces of soft tissue measuring together 1.3 × 1.0 cm., was sent for histopathological examination to the pathology department. The whole tissue was processed. The biopsy submitted was stained with haematoxylin and eosin and revealed epidermis with mild hyperkeratosis, variable degree of acanthosis and elongation of rete ridges. Papillary dermis showed numerous dilated thin-walled congested capillaries in small groups separated by thin strands of connective tissue. Histology established the diagnosis of angiokeratoma of scrotum. Follow-up period of three months to assess the cosmetic result and to look for recurrences was uneventful. Discussion Patients of angiokeratoma usually present with small, bright red, vascular papules rarely larger than 3–4 mm. Angiokeratoma of scrotum are true ectasia of blood vessels. Initially, the lesions may be red, soft and compressible but later on may be firm, keratotic and sometimes warty2. These vascular lesions may be single and discrete or arranged in clusters. The most frequent symptom is a sensation of heaviness, tension in the scrotum accompanied by irritation along with bleeding of varying degree and superadded infection. Progressive worsening of symptoms, extension of the involved area, repeated episodes of cellulitis and infection cause psychological and emotional distress in the patient; sometimes requiring hospitalisation. * Corresponding author Email: drbrijeshthakur03@gmail.com NIIMS University, Jaipur, India","PeriodicalId":19393,"journal":{"name":"OA Case Reports","volume":"87 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2013-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"OA Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.13172/2052-0077-2-11-885","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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Abstract

Introduction Angiokeratoma is a broad term that describes various conditions of asymptomatic hyperkeratotic vascular disorders with a histologic combination of hyperkeratosis and superficial dermal vascular ectasia. Here we are describing a case of recurrent angiokeratoma scroti. Case report A 34-year-old patient presented to the surgery department with multiple small papules over the scrotum with a previous history of two recurrences. They were slowly progressive, itchy and not associated with any bleeding. Examination revealed multiple soft compressible papules of 3–4 mm diameter with excoriation marks. Systemic examination and routine investigations were normal. Histologically, they were composed of numerous dilated thin walled congested capillaries mainly in the papillary dermis. Epidermis revealed variable degree of acanthosis and elongation of rete ridges and mild hyperkeratosis. Electrocauterisation of lesions was done and the follow-up period of three months was uneventful. Conclusion Although angiokeratoma scroti is not an uncommon entity, good treatment modality with minimal adverse effects in terms of complete resolution of diffuse lesions, recurrence, scarring, crusting, bleeding or cosmetic results is still not available. Introduction The term angiokeratoma is used to describe several distinct entities characterised by vascular nodules in the skin, with a histological picture of dermal vascular ectasia surmounted by hyperkeratosis of the epidermis. Angiokeratoma of the scrotum was originally described by Fordyce in 18961 reporting a case of 60-year-old man with multiple warty lesions confined to the scrotum only. Only a few cases of recurrent angiokeratoma had been reported since then. We describe here an adult male presenting with multiple papules over the scrotum with a previous history of two recurrences. Case report A 34-year-old male presented in the surgery department with moderate itching and multiple papules arranged diffusely over the scrotum. There was history of two recurrences five and three years back with the same complaints. Electrocauterisation of lesions was previously done two times, although no previous pathological reports were available. Each time, the follow-up period of four to six months had been uneventful. Even after complete post-operative healing, the patient continued to experience persistent discomfort, pruritis and psychological distress. Mere contact of the affected area with his underwear resulted in constant irritation. There was no history of trauma, episodic bleeding, similar lesions somewhere else on his body, inguinal hernia, genitourinary tumours, thrombophlebitis or varicocele. Physical examination revealed multiple, soft, bluish-red, compressible papules of 3–4 mm diameter with excoriation marks and focal thickening of skin, which might be due to previous surgical intervention. Systemic examination and routine investigations including urine examination and ultrasonography of scrotum were unremarkable. This time also, lesions were electrocauterised and excised biopsy tissue, consisting of multiple greyish white pieces of soft tissue measuring together 1.3 × 1.0 cm., was sent for histopathological examination to the pathology department. The whole tissue was processed. The biopsy submitted was stained with haematoxylin and eosin and revealed epidermis with mild hyperkeratosis, variable degree of acanthosis and elongation of rete ridges. Papillary dermis showed numerous dilated thin-walled congested capillaries in small groups separated by thin strands of connective tissue. Histology established the diagnosis of angiokeratoma of scrotum. Follow-up period of three months to assess the cosmetic result and to look for recurrences was uneventful. Discussion Patients of angiokeratoma usually present with small, bright red, vascular papules rarely larger than 3–4 mm. Angiokeratoma of scrotum are true ectasia of blood vessels. Initially, the lesions may be red, soft and compressible but later on may be firm, keratotic and sometimes warty2. These vascular lesions may be single and discrete or arranged in clusters. The most frequent symptom is a sensation of heaviness, tension in the scrotum accompanied by irritation along with bleeding of varying degree and superadded infection. Progressive worsening of symptoms, extension of the involved area, repeated episodes of cellulitis and infection cause psychological and emotional distress in the patient; sometimes requiring hospitalisation. * Corresponding author Email: drbrijeshthakur03@gmail.com NIIMS University, Jaipur, India
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复发性阴囊血管角质瘤1例
血管角化瘤是一个广义的术语,描述了各种无症状的角化过度血管疾病,组织学上伴有角化过度和表皮血管扩张。我们在此报告一例复发性阴囊血管角质瘤。病例报告一名34岁的患者在阴囊上出现多个小丘疹,既往有两次复发史。它们进展缓慢,发痒,没有出血。检查发现多个直径3-4毫米的柔软可压缩丘疹,并有擦伤痕迹。全身检查及常规检查均正常。组织学上,它们由大量扩张的薄壁充血毛细血管组成,主要分布在乳头状真皮中。表皮表现为不同程度的棘皮增生和网状脊伸长,轻度角化过度。对病变进行电灼治疗,随访3个月无意外。结论虽然阴囊血管角化瘤并不少见,但在完全消除弥漫性病变、复发、结痂、结痂、出血或美容效果方面,不良反应最小的治疗方法仍未出现。血管角化瘤这个术语被用来描述几种不同的实体,其特征是皮肤中的血管结节,具有表皮角化过度的真皮血管扩张的组织学图像。阴囊血管角化瘤最初是由Fordyce于1861年报道的一例60岁男性患者,其多发疣状病变仅局限于阴囊。从那时起,只有少数血管角质瘤复发的病例被报道。我们在这里描述一个成年男性表现为多个丘疹超过阴囊与以前的历史,两次复发。病例报告一名34岁男性,因阴囊上有中度瘙痒和多发弥漫性丘疹就诊于外科。五年前和三年前有过两次复发,都是同样的症状。电烧灼病变以前做了两次,虽然没有以前的病理报告可用。每一次,四到六个月的随访期间都平安无事。即使在完全术后愈合后,患者继续经历持续的不适,瘙痒和心理困扰。仅仅是他的内衣接触患处就会导致持续的刺激。他没有外伤史、偶发性出血、身体其他部位类似病变、腹股沟疝、泌尿生殖系统肿瘤、血栓性静脉炎或精索静脉曲张。体格检查发现多发性,软,蓝红色,可压缩丘疹,直径3-4 mm,伴有擦伤痕迹和局灶性皮肤增厚,可能是由于既往手术干预所致。全身检查和常规检查包括尿液检查和阴囊超声检查无明显差异。这一次,病变被电烧灼并切除活检组织,由多个灰白色软组织块组成,大小为1.3 × 1.0 cm。,被送到病理科做组织病理检查。整个组织都经过处理。提交的活检用血红素和伊红染色,发现表皮有轻度角化过度,不同程度的棘层和网状嵴伸长。乳头状真皮层显示大量扩张的薄壁充血毛细血管,以细链结缔组织分隔。组织学诊断为阴囊血管角化瘤。随访3个月,评估美容效果和寻找复发是平淡无奇的。血管角化瘤患者通常表现为小的鲜红色血管性丘疹,很少大于3-4毫米。阴囊血管角化瘤是真正的血管扩张。最初,病变可能是红色的、柔软的和可压缩的,但后来可能是坚硬的、角化的,有时是疣状的。这些血管病变可能是单一的、离散的,也可能排列成簇。最常见的症状是阴囊感到沉重、紧张,并伴有不同程度的出血和附加感染。症状进行性恶化,受累面积扩大,蜂窝织炎和感染反复发作,造成患者心理和情绪困扰;有时需要住院治疗。*通讯作者Email: drbrijeshthakur03@gmail.com印度斋浦尔NIIMS大学
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