Singhal Juhi, Gupta Sandeep, Agarwal Varun K, Brara Akshay, Jain Neha
Surgery, Sarojini Naidu (SN) Medical College, Agra, IND.
Surgical Oncology, Sarojini Naidu (SN) Medical College, Agra, IND.
Cureus. 2025 Apr 17;17(4):e82421. doi: 10.7759/cureus.82421. eCollection 2025 Apr.
Parasitic twins are an extremely rare condition, though their precise occurrence is unclear, with estimates suggesting a few reported cases. The parasite, the dependent, undeveloped twin, is attached to the independent, developed twin, called the autosite, at many sites. There are eight probable sites for attachment: the thoracopagus, omphalopagus, craniopagus, cephalopagus, parapagus, ischiopagus, pyopagus, and rachipagus. We report a very rare case of epigastric heteropagus in which the host's epigastrium was attached to the parasite. A 47-year-old woman presented with a progressive abdominal mass that had been present since birth. She had four alive children who were all delivered vaginally at home. The patient was found to be pale throughout general, physical, and systemic tests, with the remainder of her data being within normal ranges. Upon abdominal examination, a pedunculated enlargement measuring approximately 24 × 16 × 12 cm and exhibiting signs of a primitive face with a single ear, a nose, and limb buds was discovered. Contrast-enhanced computed tomography (CT) and CT angiography revealed a soft tissue swelling covering the patient's anterior thorax and abdomen, measuring 6.7 × 13 × 7.5 cm in size. The patient's right superior epigastric artery served as the primary vascular supply for the lesion. A parasitic epigastric heteropagus twin is a rare congenital anomaly. In such cases, it is imperative to pre-operatively assess shared organs and the feeding arterial supply in order to excise the mass in toto without compromising the hemodynamics of the host.
寄生双胞胎是一种极为罕见的情况,尽管其确切发生率尚不清楚,据估计仅有少数病例报道。寄生体,即依赖的、未发育的双胞胎,在许多部位附着于独立的、已发育的双胞胎,即自养体。可能的附着部位有八个:胸部联体、脐部联体、颅骨联体、头部联体、侧位联体、坐骨联体、脓性联体和脊柱联体。我们报告了一例非常罕见的上腹部异位联体病例,其中宿主的上腹部与寄生体相连。一名47岁女性自出生以来就有一个逐渐增大的腹部肿块。她有四个存活的孩子,都是在家中经阴道分娩的。在全身、体格和系统检查中,发现患者面色苍白,其余数据均在正常范围内。腹部检查时,发现一个带蒂肿物,大小约为24×16×12 cm,有原始面部的迹象,包括一只耳朵、一个鼻子和肢体芽。增强计算机断层扫描(CT)和CT血管造影显示,一个软组织肿胀覆盖患者的前胸和腹部,大小为6.7×13×7.5 cm。患者的右上腹上动脉是该病变的主要血管供应。寄生性上腹部异位联体双胞胎是一种罕见的先天性异常。在这种情况下,术前必须评估共享器官和供血动脉,以便完整切除肿块而不影响宿主的血流动力学。