S3763 Electrolyte Imbalance and Chronic Diarrhea: Unmasking McKittrick-Wheelock Syndrome

Introduction: McKittrick-Wheelock syndrome is an infrequent clinical condition associated with large distal colorectal tumors, usually secondary to the presence of a hypersecretory colorectal villous adenoma. Patients typically present with life-threatening hyponatremia, hypokalemia, and acute kidney injury. Timely recognition is critical, as these tumors may be the initial manifestation of an otherwise asymptomatic colorectal neoplasm. Case Description/Methods: An 81-year-old woman seeked medical consultation after experiencing watery diarrhea for the past 2 months. Physical examination revealed signs of dehydration, hypotension, tachycardia and substantial weight loss (22 lbs). She has no significant medical background and a diagnosis of chronic diarrhea was established. A digital rectal examination identified a soft, non-compressible mass. Laboratory tests indicated hyponatremia (124.0 mmol/L) and elevated creatinine (7.41 mg/dL). Subsequently, a colonoscopy was performed, which identified a laterally growing, exophytic lesion extending from the pectineal line to 8 cm from the anal verge, occupying approximately 70% of the rectal circumference. Biopsy unveiled elongated, finger-like projections extending away from the muscularis mucosae. The epithelium displayed crowded, pseudostratified cells with elongated nuclei, showing low-grade dysplasia and isolated atypia. These findings confirmed the diagnosis of a low-grade tubulovillous adenoma. Accordingly, the patient was referred to the surgical team for transanal resection. Her clinical status was stabilized, and complete excision of the lesion was achieved. The patient recovered successfully and remains in good health. Discussion: This case highlights the importance of considering McKittrick–Wheelock syndrome in the differential diagnosis of severe metabolic disturbances in patients with a history of chronic diarrhea. Recognition of this syndrome is crucial, as secretory villous adenomas may be the initial manifestation of an otherwise asymptomatic colorectal neoplasm. Villous adenomas represent approximately 5% of all colorectal adenomas, with about 3% exhibiting hypersecretory behavior, often correlated with lesion size. Therefore, chronic diarrhea should be thoroughly investigated, as it represents an alarm symptom, particularly in patients over 50 years of age. Early recognition of gastrointestinal symptoms is thus essential to facilitate timely diagnosis and management, which can significantly improve patient outcomes.

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Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001142512.04290.3d
Primary Topic
Clinical Nutrition and Gastroenterology
Type
article
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article

S3763 Electrolyte Imbalance and Chronic Diarrhea: Unmasking McKittrick-Wheelock Syndrome

Wilson Cueva, Maria Jose Cueva, Daniel Mendes Leal, Angel Cruz et al.
The American Journal of Gastroenterology
Clinical Nutrition and Gastroenterology
article

S3763 Electrolyte Imbalance and Chronic Diarrhea: Unmasking McKittrick-Wheelock Syndrome

Wilson Cueva, Maria Jose Cueva, Daniel Mendes Leal, Angel Cruz, Melissa Guillen, Francisco Cano, Sergio Manzur
article en

Abstract

Introduction: McKittrick-Wheelock syndrome is an infrequent clinical condition associated with large distal colorectal tumors, usually secondary to the presence of a hypersecretory colorectal villous adenoma. Patients typically present with life-threatening hyponatremia, hypokalemia, and acute kidney injury. Timely recognition is critical, as these tumors may be the initial manifestation of an otherwise asymptomatic colorectal neoplasm. Case Description/Methods: An 81-year-old woman seeked medical consultation after experiencing watery diarrhea for the past 2 months. Physical examination revealed signs of dehydration, hypotension, tachycardia and substantial weight loss (22 lbs). She has no significant medical background and a diagnosis of chronic diarrhea was established. A digital rectal examination identified a soft, non-compressible mass. Laboratory tests indicated hyponatremia (124.0 mmol/L) and elevated creatinine (7.41 mg/dL). Subsequently, a colonoscopy was performed, which identified a laterally growing, exophytic lesion extending from the pectineal line to 8 cm from the anal verge, occupying approximately 70% of the rectal circumference. Biopsy unveiled elongated, finger-like projections extending away from the muscularis mucosae. The epithelium displayed crowded, pseudostratified cells with elongated nuclei, showing low-grade dysplasia and isolated atypia. These findings confirmed the diagnosis of a low-grade tubulovillous adenoma. Accordingly, the patient was referred to the surgical team for transanal resection. Her clinical status was stabilized, and complete excision of the lesion was achieved. The patient recovered successfully and remains in good health. Discussion: This case highlights the importance of considering McKittrick–Wheelock syndrome in the differential diagnosis of severe metabolic disturbances in patients with a history of chronic diarrhea. Recognition of this syndrome is crucial, as secretory villous adenomas may be the initial manifestation of an otherwise asymptomatic colorectal neoplasm. Villous adenomas represent approximately 5% of all colorectal adenomas, with about 3% exhibiting hypersecretory behavior, often correlated with lesion size. Therefore, chronic diarrhea should be thoroughly investigated, as it represents an alarm symptom, particularly in patients over 50 years of age. Early recognition of gastrointestinal symptoms is thus essential to facilitate timely diagnosis and management, which can significantly improve patient outcomes.

The American Journal of GastroenterologyVol. 120(10S2)
Openalex Percentile: Top 63%
Clinical Nutrition and Gastroenterology
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