Situs inversus totalis in combination with hiatal hernia and hereditary hemolytic anemia in a 4-year-old child: A case report

Aslamkhon M. Sharipov, Nuriddin D. Mukhiddinov, Rukhshona A. Rahmatova, S. A. Mazabshoev
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Abstract

Situs inversus totalis is an extremely rare anomaly in which the organs of the chest and abdominal cavity lie in the opposite direction. With complete transposition, clinical manifestations may be absent, and diagnostic and therapeutic problems may arise in the presence of other malformations or diseases. A 4-year-old girl was admitted for treatment in the hematology department of the National Medical Center of the Republic of Tajikistan, with complaints of nausea, periodic vomiting, lethargy, lack of appetite, malaise, and skin pallor. Owing to the ineffectiveness of conservative therapy, surgical treatment was recommended, i.e., splenectomy. During the preoperative examination, radiography and radiopaque examination of the organs of the gastrointestinal tract with barium sulfate revealed that the fundus and body of the stomach were located in the left half of the chest, and the heart was symmetrically deployed to the right. An ultrasound examination revealed signs of displacement of the liver to the left half of the abdomen, the spleen to the right, and the heart in the right half of the chest. The diagnosis was hiatal hernia on the left, situs inversus totalis, hereditary hemolytic anemia, fermentopathy, and G-6-PD deficiency. Laparoscopic surgery was performed, which included splenectomy, elimination of a hiatal hernia, chiatoplasty, and esophagogastrofundoplication with the creation of a Nissen cuff. The girl was discharged on day 10. On control examination after 6 and 12 months, she had no complaints and has grown and developed according to age. This clinical case is the first in the Russian literature to describe the treatment of a child with a hiatal hernia against the background of complete transposition of internal organs. This case highlights the need for imaging techniques for any unclear symptoms, especially in children with hereditary diseases. Minimally invasive intervention could contribute to a favorable outcome.
完全性倒位合并裂孔疝和遗传性溶血性贫血1例
完全性倒位是一种非常罕见的异常,它是指胸腔和腹腔的器官位于相反的方向。完全转位时,可能没有临床表现,并且在存在其他畸形或疾病时可能出现诊断和治疗问题。一名4岁女孩在塔吉克斯坦共和国国家医疗中心血液科接受治疗,主诉恶心、周期性呕吐、嗜睡、食欲不振、不适和皮肤苍白。由于保守治疗无效,建议手术治疗,即脾切除术。术前检查胃肠脏器造影术及硫酸钡透片检查显示胃底及胃体位于左半边胸部,心脏对称向右展布。超声检查显示肝脏移至左腹部,脾脏移至右腹部,心脏移至右胸部。诊断为左侧裂孔疝、完全性倒位、遗传性溶血性贫血、发酵病和G-6-PD缺乏症。施行腹腔镜手术,包括脾切除术、裂孔疝消除术、切口成形术、食管胃底吻合及尼森袖带术。女孩于第10天出院。6个月和12个月后对照检查,患者无症状,已按年龄生长发育。这个临床病例是第一个在俄罗斯文献中描述一个儿童裂孔疝的治疗背景下完全转位的内部器官。本病例强调了对任何不明确症状的影像学检查的必要性,特别是对患有遗传性疾病的儿童。微创干预可能有助于获得良好的结果。
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