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

Aslamhon M. Sharipov , Nuriddin D. Mukhiddinov , Rukhshona A. Rahmatova , Salomatsho A. Mazabshoev

Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care ›› 2022, Vol. 12 ›› Issue (3) : 383 -390.

PDF
Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care ›› 2022, Vol. 12 ›› Issue (3) : 383 -390. DOI: 10.17816/psaic1037
Case reports
research-article

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

Author information +
History +
PDF

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.

Keywords

pediatric surgery / malformations / situs inversus totalis / hiatal hernia / hereditary hemolytic anemia / laparoscopy / children

Cite this article

Download citation ▾
Aslamhon M. Sharipov, Nuriddin D. Mukhiddinov, Rukhshona A. Rahmatova, Salomatsho A. Mazabshoev. Situs inversus totalis in combination with hiatal hernia and hereditary hemolytic anemia in a 4-year-old child: A case report. Russian Journal of Pediatric Surgery, Anesthesia and Intensive Care, 2022, 12(3): 383-390 DOI:10.17816/psaic1037

登录浏览全文

4963

注册一个新账户 忘记密码

References

[1]

Casey B. Genetics of human situs abnormalities. Am J Med Genet. 2001;101(4):356–358. DOI: 10.1002/ajmg.1220

[2]

Casey B. Genetics of human situs abnormalities // Am J Med Genet. 2001. Vol. 101, No. 4. P. 356–358. DOI: 10.1002/ajmg.1220

[3]

Sutherland MJ, Ware SM. Disorders of left-right asymmetry: heterotaxy and situs inversus. Am J Med Genet C Semin Med Genet. 2009;151C(4):307–317. DOI: 10.1002/ajmg.c.30228

[4]

Sutherland M.J., Ware S.M. Disorders of left-right asymmetry: heterotaxy and situs inversus // Am J Med Genet C Semin Med Genet. 2009. Vol. 151C, No. 4. P. 307–317. DOI: 10.1002/ajmg.c.30228

[5]

Fonkalsrud EW, Tompkins R, Clatworthy HW. Abdominal manifestations of situs inversus in infants and children. Arch Surg. 1966;92(5):791–795. DOI: 10.1001/archsurg.1966.01320230139025

[6]

Fonkalsrud E.W., Tompkins R., Clatworthy H.W. Abdominal manifestations of situs inversus in infants and children // Arch Surg. 1966. Vol. 92, No. 5. P. 791–795. DOI: 10.1001/archsurg.1966.01320230139025

[7]

Poroki razvitiya diafragmy In: Neonatal’naya khirurgiya. Yu.F. Isakov, N.N. Volodin, A.V. Geraskin, eds. Moscow: Dinastiya; 2011. P. 332–358.

[8]

Пороки развития диафрагмы // Неонатальная хирургия / под ред. Ю.Ф. Исакова, Н.Н. Володина, А.В. Гераськина. Москва: Династия, 2011. P. 332–358

[9]

McGivern MR, Best KE, Rankin J, et al. Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study. Arch Dis Child Fetal Neonatal Ed. 2015;100(2):F137–F144. DOI: 10.1136/archdischild-2014-306174

[10]

McGivern M.R., Best K.E., Rankin J., et al. Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study // Arch Dis Child Fetal Neonatal Ed. 2015. Vol. 100, No. 2. P. F137–F144. DOI: 10.1136/archdischild-2014-306174

[11]

Tesselaar CD, Postema RR, van Dooren MF, et al. Congenital diaphragmatic hernia and situs inversus totalis. Pediatrics. 2004;113(3):e256–e258. DOI: 10.1542/peds.113.3.e256

[12]

Tesselaar C.D., Postema R.R., van Dooren M.F., et al. Congenital diaphragmatic hernia and situs inversus totalis // Pediatrics. 2004. Vol. 113, No. 3. P. e256–e258. DOI: 10.1542/peds.113.3.e256

[13]

Romeo C, Turiaco N, Gitto E, et al. Right bochdalek hernia associated with kartagener syndrome: developmental and clinical observations. European J Pediatr Surg Rep. 2013;1(1):15–17. DOI: 10.1055/s-0033-1343077

[14]

Romeo C., Turiaco N., Gitto E., et al. Right bochdalek hernia associated with kartagener syndrome: developmental and clinical observations // European J Pediatr Surg Rep. 2013. Vol. 1, No. 1. P. 15–17. DOI: 10.1055/s-0033-1343077

[15]

Patel RV, Jackson P, De Coppi P, et al. Laparoscopic Nissen fundoplication and gastrostomy for a giant hiatal hernia in an infant with situs inversus totalis. BMJ Case Rep. 2014;2014:bcr2013202764. DOI: 10.1136/bcr-2013-202764

[16]

Patel R.V., Jackson P., De Coppi P., et al. Laparoscopic Nissen fundoplication and gastrostomy for a giant hiatal hernia in an infant with situs inversus totalis // BMJ Case Rep. 2014. Vol. 2014. P. bcr2013202764. DOI: 10.1136/bcr-2013-202764

[17]

Demidov VN, Mashinets NV, Gus A, et al. A rare case of congenital right-sided diaphragmatic hernia in combination with situs inversus in a fetus. Obstetrics and Gynecology. 2015;(6):136–139.

[18]

Демидов В.Н., Машинец Н.В., Гус А., и др. Редкий случай врожденной правосторонней диафрагмальной грыжи в сочетании с обратным расположением внутренних органов у плода // Акушерство и гинекология. 2015. № 6. С. 136–139.

[19]

Bogdanov AN, Mazurov VI. Hemolytic anemia. St Petersburg Medical Academy of Postgraduate Studies. 2011;3(3):107–114.

[20]

Богданов А.Н., Мазуров В.И. Гемолитические анемии // Вестник Санкт-Петербургской медицинской академии последипломного образования. 2011. Т. 3, № 3. С. 107–114.

[21]

Torfs CP, Curry CJ, Bateson TF, et al. A population-based study of congenital diaphragmatic hernia. Teratology. 1992;46(6):555–565. DOI: 10.1002/tera.1420460605

[22]

Torfs C.P., Curry C.J., Bateson T.F., et al. A population-based study of congenital diaphragmatic hernia // Teratology. 1992. Vol. 46, No. 6. P. 555–565. DOI: 10.1002/tera.1420460605

[23]

Heitmann F, Erdem S, Langwieder C, et al. Total laryngo-tracheo-esophageal cleft with situs inversus totalis, aplasia of the right diaphragm and hypoplasia of the lung on the right side. Z Geburtshilfe Perinatol. 1988;192(4):181–183. (In German.)

[24]

Heitmann F., Erdem S., Langwieder C., et al. Totale laryngo-tracheo-oesophageale Spalte in Kombination mit Situs inversus totalis // Zwerchfellaplasie rechts und Hypoplasie der rechtsseitigen Lunge. 1988. Vol. 192, No. 4. P. 181–183.

[25]

Itoh M, Wada Y, Hashimoto U, et al. A case of intralobar pulmonary sequestration associated with ASD, dextrocardia, hypoplasia of the right lung and eventration of the diaphragm. Kyobu Geka. 1987;40(13):1099–1103.

[26]

Itoh M., Wada Y., Hashimoto U., et al. A case of intralobar pulmonary sequestration associated with ASD, dextrocardia, hypoplasia of the right lung and eventration of the diaphragm // Kyobu Geka. 1987. Vol. 40, No. 13. P. 1099–1103.

[27]

Yang MJ, Russell KW, Yoder BA, Fenton SJ. Congenital diaphragmatic hernia: a narrative review of controversies in neonatal management. Transl Pediatr. 2021;10(5):1432–1447. DOI: 10.21037/tp-20-142

[28]

Yang M.J., Russell K.W., Yoder B.A., Fenton S.J. Congenital diaphragmatic hernia: a narrative review of controversies in neonatal management // Transl Pediatr. 2021. Vol. 10, No. 5. P. 1432–1447. DOI: 10.21037/tp-20-142

[29]

Mandhan P, Memon A, Memon AS. Congenital hernias of the diaphragm in children. J Ayub Med Coll Abbottabad. 2007;19(2):37–41.

[30]

Mandhan P., Memon A., Memon A.S. Congenital hernias of the diaphragm in children // J Ayub Med Coll Abbottabad. 2007. Vol. 19, No. 2. P. 37–41.

[31]

Razumovsky AYu, Alkhasov AB, Bataev SМ, Ekimovskaya EV. Laparoscopic Nissen fundoplication — the gold standard for the treatment of gastroesophageal reflux in children. Experimental and Clinical Gastroenterology. 2015;1(113):72–77.

[32]

Разумовский А.Ю., Алхасов А.Б., Батаев С.М., Екимовская Е.В. Лапароскопическая фундопликация по Ниссену — золотой стандарт лечения гастроэзофагеального рефлюкса у детей // Экспериментальная и клиническая гастроэнтерология. 2015. № 1(113). С. 72–77.

[33]

Ru W, Wu P, Feng S, et al. Laparoscopic versus open Nissen fundoplication in children: A systematic review and meta-analysis. J Pediatr Surg. 2016;51(10):1731–1736. DOI: 10.1016/j.jpedsurg.2016.07.012

[34]

Ru W., Wu P., Feng S., et al. Laparoscopic versus open Nissen fundoplication in children: A systematic review and meta-analysis // J Pediatr Surg. 2016. Vol. 51, No. 10. P. 1731–1736. DOI: 10.1016/j.jpedsurg.2016.07.012

[35]

Tsung A, Feliz A, Kane TD. Laparoscopic Nissen fundoplication in an infant with situs inversus. J Laparoendosc Adv Surg Tech A. 2007;17(5):698–700. DOI: 10.1089/lap.2006.0244

[36]

Tsung A., Feliz A., Kane T.D. Laparoscopic Nissen fundoplication in an infant with situs inversus // J Laparoendosc Adv Surg Tech A. 2007. Vol. 17, No. 5. P. 698–700. DOI: 10.1089/lap.2006.0244

RIGHTS & PERMISSIONS

Eco-Vector

AI Summary AI Mindmap
PDF

74

Accesses

0

Citation

Detail

Sections
Recommended

AI思维导图

/