medigraphic.com
SPANISH

Revista Mexicana de Cirugía Endoscópica

ISSN 1665-2576 (Print)
  • Contents
  • View Archive
  • Information
    • General Information        
    • Directory
  • Publish
    • Instructions for authors        
    • Send manuscript
  • medigraphic.com
    • Home
    • Journals index            
    • Register / Login
  • Mi perfil

2018, Number 4

<< Back Next >>

Rev Mex Cir Endoscop 2018; 19 (4)

Complicated acute appendicitis secondary to Henoch-Schönlein in adulthood: An uncommon pathology. A case report

Amarante LGD, Garza CAA, Gamboa ACM, Garmendia CG, Alanís RÓC
Full text How to cite this article

Language: Spanish
References: 14
Page: 171-175
PDF size: 226.25 Kb.


Key words:

Henoch-Schönlein disease, acute appendicitis, complications, laparoscopic appendectomy.

ABSTRACT

Introduction: Henoch-Schönlein is a self-limited autoimmune disease. It is the most frequent cause of vasculitis in the pediatric age. The presentation in adulthood is a rare occurrence, with a calculated incidence of 3.4 to 14.4 cases per million. It usually disappears spontaneously, but in some cases it may present with serious complications that may require surgical management. Acute appendicitis secondary to this disease is a rarely observed complication. Case report: A 56 years female, without a history of relevance, which began 10 days previous, presenting with abdominal colic type pain in mesogastrium, which subsequently migrated to both iliac crests, accompanied by arthralgias and exanthemathic lesions not itchy on both lower limbs. Physical examination showed data of peritoneal irritation at the lower abdomen. The CT showed abscesses in the pelvic cavity and right iliac fossa. She was schedule for a laparoscopic appendectomy, finding a large abscess in right iliac fossa and others between the intestinal loops. The appendix was perforated at its base and detached from the cecum with necrosis and gangrene. Partial cecum resection and abscess drainage were performed without complications. Once the abdominal sepsis was resolved, histopathological study of the lesions was performed, and in conjunction with results of laboratory studies, Henoch-Schönlein disease was diagnosed. Conclusion: Henoch-Schönlein is a rare disease in adults, abdominal manifestations that are associated with this disease should be diagnosed early because of its high morbidity-mortality when delaying treatment. Although appendicitis secondary to this type of disease is a rare pathology, it is feasible to be treated by laparoscopic appendectomy and should be taken into account for differential diagnosis.


REFERENCES

  1. Micheletti RG, Werth VP. Small vessel vasculitis of the skin. Rheum Dis Clin North Am. 2015; 41: 21-32, vii.

  2. Hung SP, Yang YH, Lin YT, Wang LC, Lee JH, Chiang BL. Clinical manifestations and outcomes of Henoch-Schönlein purpura: comparison between adults and children. Pediatr Neonatol. 2009; 50: 162-168.

  3. Kang Y, Park JS, Ha YJ, Kang MI, Park HJ, Lee SW et al. Differences in clinical manifestations and outcomes between adult and child patients with Henoch-Schönlein purpura. J Korean Med Sci. 2014; 29: 198-203.

  4. Yang YH, Yu HH, Chiang BL. The diagnosis and classification of Henoch-Schönlein purpura: an updated review. Autoimmun Rev. 2014; 13: 355-358.

  5. Sartelli M, Chichom-Mefire A, Labricciosa FM, Hardcastle T, Abu-Zidan FM, Adesunkanmi AK et al. The management of intra-abdominal infections from a global perspective: 2017 WSES guidelines for management of intra-abdominal infections. World J Emerg Surg. 2017; 12: 29. doi: 10.1186/s13017-017-0141-6.

  6. Ramírez-Terán AL, Vega-Memije ME, Toussaint-Caire S, Soto V. Púrpura de Henoch-Schönlein. Med Int Méx. 2017; 33: 285-290.

  7. Colleter L, Corcos O, Vilgrain V, Ronot M. Henoch-Schönlein purpura in adults. Diagn Interv Imaging. 2014; 95: 637-640.

  8. Semeena N, Adlekha S. Henoch-Schönlein purpura associated with gangrenous appendicitis: a case report. Malays J Med Sci. 2014; 21: 71-73.

  9. Jasić M, Subat-Dezulović M, Nikolić H, Jonjić N, Manestar K, Dezulović M. Henoch-Schönlein purpura complicated by appendicitis, intussusception and ureteritis. Coll Antropol. 2011; 35: 197-201.

  10. Jithpratuck W, Elshenawy Y, Saleh H, Youngberg G, Chi DS, Krishnaswamy G. The clinical implications of adult-onset Henoch-Schönlein purpura. Clin Mol Allergy. 2011; 9: 9.

  11. Sheth K, Bockorny M, Elaba Z, Scola C. Adult onset Henoch-Schönlein purpura: case report and review of literature. Conn Med. 2015; 79: 81-85.

  12. Lerkvaleekul B, Treepongkaruna S, Saisawat P, Thanachatchairattana P, Angkathunyakul N, Ruangwattanapaisarn N et al. Henoch-Schönlein purpura from vasculitis to intestinal perforation: A case report and literature review. World J Gastroenterol. 2016; 22: 6089-6094.

  13. Hong J, Yang HR. Laboratory markers indicating gastrointestinal involvement of Henoch-Schönlein purpura in children. Pediatr Gastroenterol Hepatol Nutr. 2015; 18: 39-47.

  14. McClain DM, Maino K, Dwyer TX. Henoch-Schönlein purpura in an adult Filipino man: a case report and literature review. Cutis. 2006; 77: 236-240.




2020     |     www.medigraphic.com

Mi perfil

C?MO CITAR (Vancouver)

Rev Mex Cir Endoscop. 2018;19