Congenital chylous as cites in a 3-month-old infant in Zaria: A case report

S. Abdullahi, H. Idris, S. Mado, A. Sadiku, A. Alfa, E. Abubakar, Y. Adzu, A. Suleiman
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Abstract

Congenital chylous ascites (CCA) is a rare disease that results from the maldevelopment of the intra-abdominal lymphatic system. Due to the rarity of congenital chylous ascites and the lack of standards in diagnosis and therapy, this disease constitutes a medical challenge and individual therapy seems to be extremely important. A 3-month-old girl diagnosed with congenital chylous ascites. She was managed initially with nil per oral, parenteral nutrition, medium chain triglyceride (MCT) containing oil and abdominal paracentesis, followed by octreotide. Medium chain triglyceride formula, the main stay of management was discontinued with gradual reintroduction of breast feeds. This case was selected due to the rarity of CCA and the lack of standards in the diagnosis and therapy.
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扎里亚3个月婴儿先天性乳糜泻1例报告
先天性乳糜腹水(CCA)是一种罕见的疾病,由腹内淋巴系统发育不良引起。由于先天性乳糜腹水的罕见性和缺乏标准的诊断和治疗,这种疾病构成了一个医学挑战,个体化治疗似乎非常重要。一个3个月大的女婴被诊断为先天性乳糜性腹水。她最初接受零剂量口服、肠外营养、中链甘油三酯(MCT)含油和腹部穿刺治疗,随后使用奥曲肽。中链甘油三酯配方,管理的主要停留停止与逐步重新引入母乳喂养。本病例因CCA罕见,诊断及治疗缺乏标准而被选择。
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