A Peculiar Accessory Scrotum With a Human Tail-Like Structure: A Case Report.

IF 0.4 Q4 PATHOLOGY
Case Reports in Pathology Pub Date : 2026-07-27 eCollection Date: 2026-01-01 DOI:10.1155/crip/9623598
Hiroshi Sonobe, Rika Omote, Ryutaro Kondo, Souji Ibuka, Ryuta Saka, Shun Iwasaki, Taku Yamamichi
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Abstract

Accessory scrotum is a rare congenital anomaly resulting from aberrant scrotal development. It is usually present at birth in the perineum of male infants and is often associated with a lipoma at its base. Here, we report a peculiar case of an accessory scrotum present at birth on the skin adjacent to the anus. The accessory scrotum was continuous with a narrow stalk consisting of longitudinally oriented connective tissue and nerve bundles within the fatty tissue, which further extended to a terminal nodule containing articular cartilage and marrow tissues in the ischiorectal fossa, forming a 7-cm-long structure. The components of the stalk and terminal nodule resembled those described in the human tail but ran subcutaneously without a skin covering. Therefore, the lesion was diagnosed as an accessory scrotum with a human tail-like structure. The lesion was completely resected at 10 months of age. Preoperative whole-body computed tomography revealed no other anomalies, and the infant demonstrated normal development approximately 1 year postoperatively. To our knowledge, no similar cases have been reported, and its histogenesis remains unexplained. We postulated that this lesion may result from the ectopic migration of pluripotent cells derived from the tail bud during early embryonic development. This case provides unique insights into the shared embryological mechanisms between accessory scrotum and human tail-like anomalies.

具有人类尾巴状结构的特殊附属阴囊一例报告。
摘要副阴囊是一种罕见的由阴囊发育异常引起的先天性异常。它通常出现于男婴出生时的会阴,并常伴有会阴底部的脂肪瘤。在这里,我们报告一个特殊的情况下,副阴囊出现在出生皮肤邻近肛门。副阴囊呈连续状,由纵向取向的结缔组织和脂肪组织内的神经束组成的窄柄,进一步延伸至坐骨直肠窝含有关节软骨和骨髓组织的末端结节,形成7 cm长的结构。茎和末端结节的组成部分类似于人类尾巴,但在皮下没有皮肤覆盖。因此,病变被诊断为副阴囊,具有人类尾巴状结构。病变在10个月大时被完全切除。术前全身计算机断层扫描未发现其他异常,术后约1年婴儿发育正常。据我们所知,没有类似病例的报道,其组织发生仍未解释。我们推测这种损伤可能是由胚胎早期发育过程中来自尾芽的多能细胞的异位迁移引起的。本病例为副阴囊和人类尾巴样畸形之间的共同胚胎学机制提供了独特的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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20
审稿时长
12 weeks
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