Ibuka Souji, Saka Ryuta, Sonobe Hiroshi, Tsukada Ryo, Iwasaki Shun, Omote Rika
Department of Pediatric Surgery, NHO Fukuyama Medical Center, 4-14-17, Okinogami-Cho, Fukuyama, Hiroshima, 720-8520, Japan.
Department of Diagnostic Pathology, NHO Fukuyama Medical Center, Fukuyama, Hiroshima, Japan.
Surg Case Rep. 2024 May 1;10(1):106. doi: 10.1186/s40792-024-01906-w.
Accessory scrotum is a congenital scrotal anomaly that is usually located anterior to the anus and frequently presents with a lipoma in a bead-like shape. Herein, we present an unusual case of an accessory scrotum with a lipoma connected by a narrow stalk and located posterior to the anus.
A 1-month-old boy was referred to our hospital for a perineal mass present at birth. He was born at 37 weeks and 2 days, with a birth weight of 2962 g. No abnormalities occurred during the perinatal period, and the birth was uneventful. The mass had an unusual shape, comprising two masses connected by a narrow stalk. The base of the mass was posterior to the anus and was connected to the rectal mucosa. The proximal mass was elastic and soft without skinfolds, whereas the distal mass was elastic and soft with a scrotum-like skinfolds. Magnetic resonance imaging showed no spina bifida. High-intensity adipose tissues in both masses and low-intensity vessels or fibrous stroma in cord-like structures between the two masses were found on T2-weighted images. At 3 months of age, the patient underwent resection in the prone jackknife position. No tumorous lesions were connected to the mass on the rectal and coccyx sides, and the mass was completely removed, preserving the anal sphincter. Histologically, the distal mass had characteristics of a scrotum, whereas the proximal mass was exclusively a lipoma. The connecting stalk had normal skin structures and a blood vessel with parallel-running nerve bundles. The postoperative course was uneventful, and the patient was discharged on postoperative day 6.
This case of accessory scrotum was unusual in its location and the presence of a stalk connecting the accessory scrotum and lipoma. The mechanism underlying accessory scrotum development remains unclear, and our report may impact the discourse regarding the embryological development of the accessory scrotum.
副阴囊是一种先天性阴囊异常,通常位于肛门前方,且常伴有珠状脂肪瘤。在此,我们报告一例罕见的副阴囊病例,其脂肪瘤通过狭窄的蒂相连,且位于肛门后方。
一名1个月大的男婴因出生时即存在会阴部肿物被转诊至我院。他于孕37周2天出生,出生体重2962克。围产期无异常情况,分娩过程顺利。肿物形状异常,由两个通过狭窄蒂相连的肿块组成。肿块基部位于肛门后方,与直肠黏膜相连。近端肿块质地弹性且柔软,无皮肤褶皱,而远端肿块质地弹性且柔软,有类似阴囊的皮肤褶皱。磁共振成像显示无脊柱裂。在T2加权图像上,两个肿块均可见高强度脂肪组织,两个肿块之间的条索状结构中有低强度血管或纤维基质。患儿3个月大时,在俯卧折刀位接受了切除术。直肠和尾骨侧的肿块未与任何肿瘤性病变相连,肿块被完全切除,同时保留了肛门括约肌。组织学检查显示,远端肿块具有阴囊特征,而近端肿块仅为脂肪瘤。连接蒂具有正常的皮肤结构以及一条伴有平行走行神经束的血管。术后过程顺利,患者于术后第6天出院。
该例副阴囊病例在位置以及存在连接副阴囊和脂肪瘤的蒂方面均较为罕见。副阴囊发育的潜在机制尚不清楚,我们的报告可能会影响有关副阴囊胚胎发育的讨论。