Medicine:McKittrick–Wheelock syndrome
| McKittrick-Wheelock syndrome | |
|---|---|
| Specialty | Gastroenterology |
McKittrick-Wheelock syndrome is an uncommon syndrome caused by large, villous adenomas that secrete high quantities of electrolyte-rich mucin. This may lead to pre-renal acute kidney injury, secretory diarrhea, and dehydration. It is estimated that 2-3% of large villous adenomas, typically greater than 4 cm in diameter, will present with this hypersecretory pattern.[1]
Symptoms and Signs
Patients typically present with a history of chronic, watery diarrhea. Before the cause is established, they may have multiple hospitalizations for dehydration and kidney failure. Patients may present with hyponatremia, hypokalemia, and elevated creatinine.[2]
Diagnosis
Treatment
The treatment is supportive until the villous adenoma can be resected surgically.[citation needed]
History
The syndrome was first described by Leland S. McKittrick and Frank C. Wheelock. In 1954 they reported a case of an 84-year-old woman with a large villous papilloma of the rectum, who presented with weakness, syncope and oliguria.[3]
See also
- Colorectal cancer
- Sessile serrated adenoma
- Tubulovillous adenoma
References
- ↑ Popescu, A et al. (2005). "McKittrick-Wheelock syndrome: a rare cause of acute renal failure". Rom J Gastroenterology 14: 63–66. PMID 15800695.
- ↑ Raphael, M; McDonald, C; Detsky, A (2015). "McKittrick-Wheelock syndrome". CMAJ 187 (9): 676–678. doi:10.1503/cmaj.141195. PMID 25754711.
- ↑ McKittrick, LS; Wheelock, FC (1954). Carcinoma of the Colon. Charles C Thomas. pp. 61–63.
 |  |
