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Akut peritonit sırasında tesadüfen fark edilen konjenital izole asplenia

Year 2020, Volume: 4 Issue: 1, 93 - 95, 02.01.2020
https://doi.org/10.28982/josam.588198

Abstract

Çok nadir görülen bir durum olan konjenital aspleninin 2 farklı tipi vardır: heterotaksi sendromları ve izole konjenital aspleni (ICA). Ivemark sendromu, asplenia, kalbin malformasyonları ve göğüs ve karındaki iç organların malpozisyonu ile karakterize heterotaksi sendromlarından biridir. ICA vakaları çocuklukta da ölümcüldür, ancak bildirilen canlı yetişkin vakaları mevcuttur. Etkilenenler tipik olarak fulminan sepsis için yüksek risk altındadır ve trombositoz ve mezenterik tromboz gibi bulaşıcı olmayan komplikasyon riski daha yüksektir. Burada ülser perforasyonuna bağlı peritonit için acil bir laparotomi sırasında tesadüfen saptanan doğuştan asplenisi olan bir hastanın olağandışı olgusunu sunuyoruz.

References

  • 1. Ahmed SA, Zengeya S, Kini U, Pollard AJ. Familial isolated congenital asplenia: Case report and literature review. Eur J Pediatr. 2010;169(3):315–8.
  • 2. Arnautovic JZ, Mazhar A, Tereziu S, Gupta K. A Rare Association of Congenital Asplenia with Jejunal Arteriovenous Malformation. The American Journal of Case reports. 2017;18:1118.
  • 3. Gilbert B, Menetrey C, Belin V, Brosset P, de Lumley L, Fisher A. Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others. Eur J Pediatr. 2002;161:368–72.
  • 4. Schutze GE, Mason EO, Jr Barson WJ, Kim KS, Wald ER, Givner LB, et al. Invasive pneumococcal infections in children with asplenia. Pediatr Infect Dis J. 2002;21:278–82.
  • 5. Halbertsma FJJ, Neeleman C, Weemaes CM, Van Deuren, M. The absent and vanishing spleen: congenital asplenia and hyposplenism—two case reports. Acta Paediatrica. 2005;94(3):369-71.
  • 6. Mahlaoui N, Minard-Colin V, Picard C, et al. Isolated congenital asplenia: A French nationwide retrospective survey of 20 cases. J Pediatr. 2011;158(1):142–8.
  • 7. Bolze A, Mahlaoui N, Byun M et al. Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia. Science. 2013;340:976–8.
  • 8. Ferlicot S, Emile JF, Le Bris JL, et al. L’asplenie congenitale: Un deficit im- munitaire de l’enfant de decouverte souvent trop tardive. Ann Path. 1997;17:44–6.
  • 9. Gonzalez M, Collaud S, Gervaz P, Morel, P. Asplenie congenitale (syndrome d’Ivemark) revelee par une thrombose veineuse mesenterique chez un malade de 77 ans. Gastroenterologie Clinique et Biologique. 2007;31(10):860-2.
  • 10. Ferlicot S, Emile JF, Le Bris JL, Cheron G, Brousse N. Congenital asplenia. A childhood immune deficit often detected too late. Ann Pathol. 1997;17:44-6.
  • 11. Myerson RM, Koelle WA: Congenital absence of the spleen in an adult: Report of a case associated with recurrent Waterhouse-Friderichsen syndrome. N Engl J Med. 1956;254(24):1131-2.
  • 12. Vincentelli C, Molina EG, Robinson MJ. Fatal pneumococcal Waterhouse- Friderichsen syndrome in a vaccinated adult with congenital asplenia. Am J Emerg Med. 2009;27(751):e3–5.
  • 13. Rose C, Quesnel B, Facon T, et al. Congenital asplenia, a different dignosis of essential thrombocythemia. Presse Med. 1993;22(34):1748.
  • 14. Lindor NM, Smithson WA, Ahumada CA et al: Asplenia in two father-son pairs. Am J Med Genet, 1995; 56(1):10-1.
  • 15. Takahashi F, Uchida K, Nagaoka T, et al. Isolated congenital spleen agenesis: A rare cause of chronic thromboembolic pulmonary hypertension in an adult. Respirology. 2008; 13:913-5.

Congenital isolated asplenia accidentally discovered during acute peritonitis

Year 2020, Volume: 4 Issue: 1, 93 - 95, 02.01.2020
https://doi.org/10.28982/josam.588198

Abstract

An extremely rare condition, congenital asplenia has 2 distinct types: heterotaxy syndromes and isolated congenital asplenia (ICA). Ivemark syndrome is one of the heterotaxy syndromes characterized by asplenia, malformations of the heart, and malposition of internal organs in the chest and abdomen. ICA cases are also fatal in childhood, but there are reported living adult cases. Those affected are typically at increased risk for fulminant sepsis and carry a higher risk of noninfectious complications, such as thrombocytosis and mesenteric thrombosis. We herein report the unusual case of a patient with congenital asplenia, which was discovered fortuitously during an emergency laparotomy for peritonitis due to ulcer perforation.

References

  • 1. Ahmed SA, Zengeya S, Kini U, Pollard AJ. Familial isolated congenital asplenia: Case report and literature review. Eur J Pediatr. 2010;169(3):315–8.
  • 2. Arnautovic JZ, Mazhar A, Tereziu S, Gupta K. A Rare Association of Congenital Asplenia with Jejunal Arteriovenous Malformation. The American Journal of Case reports. 2017;18:1118.
  • 3. Gilbert B, Menetrey C, Belin V, Brosset P, de Lumley L, Fisher A. Familial isolated congenital asplenia: a rare, frequently hereditary dominant condition, often detected too late as a cause of overwhelming pneumococcal sepsis. Report of a new case and review of 31 others. Eur J Pediatr. 2002;161:368–72.
  • 4. Schutze GE, Mason EO, Jr Barson WJ, Kim KS, Wald ER, Givner LB, et al. Invasive pneumococcal infections in children with asplenia. Pediatr Infect Dis J. 2002;21:278–82.
  • 5. Halbertsma FJJ, Neeleman C, Weemaes CM, Van Deuren, M. The absent and vanishing spleen: congenital asplenia and hyposplenism—two case reports. Acta Paediatrica. 2005;94(3):369-71.
  • 6. Mahlaoui N, Minard-Colin V, Picard C, et al. Isolated congenital asplenia: A French nationwide retrospective survey of 20 cases. J Pediatr. 2011;158(1):142–8.
  • 7. Bolze A, Mahlaoui N, Byun M et al. Ribosomal protein SA haploinsufficiency in humans with isolated congenital asplenia. Science. 2013;340:976–8.
  • 8. Ferlicot S, Emile JF, Le Bris JL, et al. L’asplenie congenitale: Un deficit im- munitaire de l’enfant de decouverte souvent trop tardive. Ann Path. 1997;17:44–6.
  • 9. Gonzalez M, Collaud S, Gervaz P, Morel, P. Asplenie congenitale (syndrome d’Ivemark) revelee par une thrombose veineuse mesenterique chez un malade de 77 ans. Gastroenterologie Clinique et Biologique. 2007;31(10):860-2.
  • 10. Ferlicot S, Emile JF, Le Bris JL, Cheron G, Brousse N. Congenital asplenia. A childhood immune deficit often detected too late. Ann Pathol. 1997;17:44-6.
  • 11. Myerson RM, Koelle WA: Congenital absence of the spleen in an adult: Report of a case associated with recurrent Waterhouse-Friderichsen syndrome. N Engl J Med. 1956;254(24):1131-2.
  • 12. Vincentelli C, Molina EG, Robinson MJ. Fatal pneumococcal Waterhouse- Friderichsen syndrome in a vaccinated adult with congenital asplenia. Am J Emerg Med. 2009;27(751):e3–5.
  • 13. Rose C, Quesnel B, Facon T, et al. Congenital asplenia, a different dignosis of essential thrombocythemia. Presse Med. 1993;22(34):1748.
  • 14. Lindor NM, Smithson WA, Ahumada CA et al: Asplenia in two father-son pairs. Am J Med Genet, 1995; 56(1):10-1.
  • 15. Takahashi F, Uchida K, Nagaoka T, et al. Isolated congenital spleen agenesis: A rare cause of chronic thromboembolic pulmonary hypertension in an adult. Respirology. 2008; 13:913-5.
There are 15 citations in total.

Details

Primary Language English
Subjects Surgery
Journal Section Case report
Authors

Elmarouni Abdelouhab 0000-0003-2035-7982

Karam Azız 0000-0002-3330-7311

Et-tayeb Ouzzanı 0000-0003-2977-2904

Ahmed Zerhounı This is me 0000-0001-8441-016X

Tarik Souıkı 0000-0001-5657-7253

Karim Ibn Majdoub El Hassanı This is me 0000-0002-0421-7296

Khalid Mazaz This is me 0000-0001-7779-7802

Imane Toughraı This is me 0000-0003-0401-3012

Publication Date January 2, 2020
Published in Issue Year 2020 Volume: 4 Issue: 1

Cite

APA Abdelouhab, E., Azız, K., Ouzzanı, E.-t., Zerhounı, A., et al. (2020). Congenital isolated asplenia accidentally discovered during acute peritonitis. Journal of Surgery and Medicine, 4(1), 93-95. https://doi.org/10.28982/josam.588198
AMA Abdelouhab E, Azız K, Ouzzanı Et, Zerhounı A, Souıkı T, Ibn Majdoub El Hassanı K, Mazaz K, Toughraı I. Congenital isolated asplenia accidentally discovered during acute peritonitis. J Surg Med. January 2020;4(1):93-95. doi:10.28982/josam.588198
Chicago Abdelouhab, Elmarouni, Karam Azız, Et-tayeb Ouzzanı, Ahmed Zerhounı, Tarik Souıkı, Karim Ibn Majdoub El Hassanı, Khalid Mazaz, and Imane Toughraı. “Congenital Isolated Asplenia Accidentally Discovered During Acute Peritonitis”. Journal of Surgery and Medicine 4, no. 1 (January 2020): 93-95. https://doi.org/10.28982/josam.588198.
EndNote Abdelouhab E, Azız K, Ouzzanı E-t, Zerhounı A, Souıkı T, Ibn Majdoub El Hassanı K, Mazaz K, Toughraı I (January 1, 2020) Congenital isolated asplenia accidentally discovered during acute peritonitis. Journal of Surgery and Medicine 4 1 93–95.
IEEE E. Abdelouhab, K. Azız, E.-t. Ouzzanı, A. Zerhounı, T. Souıkı, K. Ibn Majdoub El Hassanı, K. Mazaz, and I. Toughraı, “Congenital isolated asplenia accidentally discovered during acute peritonitis”, J Surg Med, vol. 4, no. 1, pp. 93–95, 2020, doi: 10.28982/josam.588198.
ISNAD Abdelouhab, Elmarouni et al. “Congenital Isolated Asplenia Accidentally Discovered During Acute Peritonitis”. Journal of Surgery and Medicine 4/1 (January 2020), 93-95. https://doi.org/10.28982/josam.588198.
JAMA Abdelouhab E, Azız K, Ouzzanı E-t, Zerhounı A, Souıkı T, Ibn Majdoub El Hassanı K, Mazaz K, Toughraı I. Congenital isolated asplenia accidentally discovered during acute peritonitis. J Surg Med. 2020;4:93–95.
MLA Abdelouhab, Elmarouni et al. “Congenital Isolated Asplenia Accidentally Discovered During Acute Peritonitis”. Journal of Surgery and Medicine, vol. 4, no. 1, 2020, pp. 93-95, doi:10.28982/josam.588198.
Vancouver Abdelouhab E, Azız K, Ouzzanı E-t, Zerhounı A, Souıkı T, Ibn Majdoub El Hassanı K, Mazaz K, Toughraı I. Congenital isolated asplenia accidentally discovered during acute peritonitis. J Surg Med. 2020;4(1):93-5.