Limy Bile Syndrome: A Report of a Rare Case.
Autor: | Rahate NP; Radiology, Jawaharlal Nehru Medical College, Wardha, IND., Rahate PV; Surgery, Seven Star Hospital, Nagpur, IND. |
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Jazyk: | angličtina |
Zdroj: | Cureus [Cureus] 2022 Jul 30; Vol. 14 (7), pp. e27473. Date of Electronic Publication: 2022 Jul 30 (Print Publication: 2022). |
DOI: | 10.7759/cureus.27473 |
Abstrakt: | Milk of Calcium Bile or Limy Bile Syndrome (LBS) is a sporadic and infrequent complication of cholecystitis in which the gallbladder is filled with radio-opaque, abnormal bile secretion. A 40-year-old female came to a tertiary care hospital with symptoms of recurrent pain upper abdomen for two years. On examination, the patient had mild jaundice and mild tenderness at Murphy's point exacerbated on deep inspiration. Laboratory investigations suggested raised levels of bilirubin and hepatic enzymes. Upper GI endoscopy revealed a normal GI tract. A hepatobiliary iminodiacetic acid-cholecystokinin (HIDA-CCK) scan suggested a gallbladder ejection fraction of 5%. Cholecystectomy was done the next day. Infrared imaging under Indocyanine green (ICG) dye revealed a completely dark gallbladder. The patient was asked to take ursodeoxycholic acid preparation post-operatively for four weeks. This case of LBS was discharged on the third postoperative day. She was asked to regularly follow up with the surgeons. LBS is a rare patho-clinical entity with a need for standardized diagnostic and treatment regimen. Further case reporting and studies are required to understand the disease in more depth. Competing Interests: The authors have declared that no competing interests exist. (Copyright © 2022, Rahate et al.) |
Databáze: | MEDLINE |
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