Ugwu Jideofor Okechukwu, Onwukamuche Michael Emeka, Ekwunife Hyginus O, C Emejulu Jude Kennedy, Modekwe Victor, Osuigwe Osuigwe An
Department of Surgery, Paedaitric Surgery Unit, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Nigeria.
Department of Histopathology, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Nigeria.
Niger J Surg. 2017 Jul-Dec;23(2):141-144. doi: 10.4103/njs.NJS_57_16.
Malignant peripheral nerve sheath tumor is a rare tumor occurring in 5%-10% of all malignant soft tissues sarcomas and triton tumor arising from neurofibromatosis type 1 (NF-1) is even rarer with associated high rate of mortality. No case of triton tumor has been reported in Nigeria to the best of our knowledge. We seek to report a case of lately detected retroperitoneal triton tumor presenting in a 12-year-old Nigerian child who was brought with bilateral lower limb weaknesses, weight loss, and a right lumbar mass. There were multiple café au lait spots on the body. Abdominal computerized tomographic scan revealed a huge right retroperitoneal mass crossing the midline, compressing adjacent structures with multilevel intraspinal extensions. Core needle biopsy performed and both histology and immunohistochemical studies confirmed the diagnosis, but patient demised in the course of care. The aim is to heighten suspicion of this extremely very rare malignant tumor in children with NF-1.
恶性外周神经鞘瘤是一种罕见的肿瘤,占所有恶性软组织肉瘤的5%-10%,而源自1型神经纤维瘤病(NF-1)的蝾螈瘤则更为罕见,且死亡率很高。据我们所知,尼日利亚尚未报告过蝾螈瘤病例。我们报告一例最近发现的腹膜后蝾螈瘤病例,该病例发生在一名12岁的尼日利亚儿童身上,该儿童因双侧下肢无力、体重减轻和右腰部肿块前来就诊。身体上有多个牛奶咖啡斑。腹部计算机断层扫描显示,一个巨大的右腹膜后肿块越过中线,压迫相邻结构,并向脊髓内多节段延伸。进行了粗针活检,组织学和免疫组织化学研究均确诊,但患者在治疗过程中死亡。目的是提高对NF-1儿童中这种极其罕见的恶性肿瘤的警惕性。