Abstract
We report the pediatric case of xanthogramulomatous cholecystitis. It is the first case recognized laparoscopically in the world literature. Attention is drawn to the distinctive laparoscopic features, as well as the potential hazards of laparoscopic removal. Serial ultrasound studies in our case demonstrated the evolution of the xanthogranulomatous process.
Similar content being viewed by others
References
Roberts KM, Parsons MA (1987) Xanthogranulomatous cholecystitis: clinicopathological study of 13 cases. J Clin Pathol 40: 412–417
Takahashi K, Oka K, Hakozaki H, Kojima M (1976) Ceroid-like histiocytic granuloma of gall bladder. Acta Pathol Jpn 26: 25–46
Ayling RM, Heaton ND, Davenport, Driver M, Howard ER (1993) Xanthogranulomatous cholecystitis in a 10-year-old boy. Pediatr Surg Int 8: 170–172
Fligiel S, Lewin KJ (1982) Xanthogranulomatous cholecystitis. Arch Pathol Lab Med 106: 302–304
Christensen AH, Ishak KG (1970) Benign tumors and pseudotumors of the gallbladder. Arch Pathol 90: 423–432
Goodman ZD, Ishak KG (1981) Xanthogranulomatous cholecystitis. Am J Surg Pathol 5: 653–659
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Ng, W.T., Cheng, D. & Yuen, W.F. Xanthogranulomatous cholecystitis. Pediatr Surg Int 10, 386–388 (1995). https://doi.org/10.1007/BF00182233
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00182233