Atma Jaya Neuroscience and Cognitive Center (ANCC), School of Medicine and Health Sciences, Atma Jaya Catholic University of Indonesia, Jakarta, Indonesia.
Emergency Department, Bunda Pengharapan Hospital, Merauke, South Papua, Indonesia.
Childs Nerv Syst. 2024 Aug;40(8):2631-2635. doi: 10.1007/s00381-024-06440-6. Epub 2024 May 2.
Conjoined twins (CT), which used to be historically defined as "monstrous human" and previously so-called Siamese twins in the early eighteenth century, are one of the very rare congenital malformations with an uncertain etiology and complex yet remain inconclusively debatable regarding its pathophysiological mechanisms of fusion and fission theories. Among all types of CT, parasitic CT, especially the pygopagus sub-type, is exceedingly rarer. To the best of the authors' knowledge, no parasitic CT had been reported in Papua, and this is the first finding in South Papua.
Herein, a 30-year-old multigravida female with 37th-week gestation, previous twice spontaneous miscarriage, and non-adequate antenatal care history is presented with a chief complaint of painful construction and greenish fluid leakage from the vagina, with an examination that showed a cephalic presentation with a "peculiar" big mass at the upper uterus and complete cervical dilation toward second-stage inpartu. Vaginal delivery was performed with a complication of obstructed labor due to uncommon dystocia with a suspected "big mass" below the fetal buttocks and intrapartum dead. Intrapartum transabdominal ultrasound demonstrates a gross anatomically like an organ inside a fluid-filled mass with unidentified parts, leading to a suspected type of congenital malformation at the baby's sacral region. Emergency C-section was done with findings of parasitic pygopagus CT, showing an attachment of a large irregular fluid-filled mass-like incomplete twin (parasite) with palpable soft tissue and bony structure inside to the buttocks of a male autosite twin, and an additional third leg which happened to be an under-developed lower extremity with a sacrum-like structure.
An obstetrician's routine ANC and critical radiological evaluation will increase the odds of identifying CT or other congenital malformations to provide better delivery planning or further management. Increasing maternal health knowledge in society, improving medical skills and knowledge levels for health providers, and advancing supporting facilities and specialists are future strategies for managing and preventing such cases in low-middle-income countries.
联体双胞胎(CT)曾在历史上被定义为“畸形人”,在 18 世纪早期被称为暹罗双胞胎,是一种非常罕见的先天性畸形,其病因不确定,融合和分裂理论的病理生理学机制也很复杂,但仍存在争议。在所有类型的 CT 中,寄生 CT 尤其是臀位联体更为罕见。据作者所知,在巴布亚还没有报告过寄生 CT,这是在南巴布亚的首次发现。
本文介绍了一位 30 岁的多产妇,孕 37 周,有两次自然流产史,且产前检查不充分,主要症状为阴道疼痛和绿色液体漏出,检查发现胎头先露,子宫上部有一个“奇特”的大肿块,宫颈完全扩张至第二产程。阴道分娩时,由于胎儿臀部下方的难产和分娩过程中死胎,出现了产程受阻的并发症。分娩过程中的经腹超声显示,一个大的解剖结构类似一个充满液体的肿块,有未识别的部分,导致婴儿骶骨区域疑似先天性畸形。紧急行剖宫产术,发现寄生臀位联体 CT,附着于一个大的不规则充满液体的肿块状不完全双胞胎(寄生虫),可触及内部软组织和骨性结构,附着于男性自体双胞胎的臀部,还有第三条腿,实际上是发育不良的下肢,有类似骶骨的结构。
产科医生常规的 ANC 和关键的影像学评估将增加识别 CT 或其他先天性畸形的可能性,从而提供更好的分娩计划或进一步的管理。提高社会对产妇健康知识的认识,提高卫生提供者的医疗技能和知识水平,以及推进支持设施和专家,是中低收入国家管理和预防此类病例的未来策略。