The association of gastrointestinal polyposis, alopecia, and nail dystrophy was first reported by Cronkhite and Canada (1955). Since then, to the best of our knowledge, 21 other cases of Caucasian have been reported (1977). In Japan, 32 cases of Japanese have been reported. This paper presents a case of Cronkite-Canada syndrome and the endoscopical studies of the upper G-I tract, and reviewed the literatures with reference to the clinical aspects. The patient, a 61 year-old male, was admitted with complaints of taste disorder, nail deformities, and general malaise in April, 1978. Five years before admission, the patient had the same complaints and a gastrectomy was performed under a diagnosis of gastric polyposis. Immediately after the operation, all fingernails and toenails became brittle and were broken off. His family history was negative for gastrointestinal and dermal diseases. On physical examination, alopecia, hyperpigmentation of the skin, nail deformities were noted. Laboratory findings revealed iron deficiency anemia, lactase deficiency, disturbed V.B12 absorption due to intrinsic factor deficiency. But, serum protein and electrolytes levels were within normal limits. Gordon test was, also, normal. Although primary hypothyroidism was sus-pected because of elevated fasting level of serum TSH, it could not be examined further. Röntgenograms showed multiple small filling defects in the gastric stump and large intestine, and polyposis in the entire duodenum and a part of the ileum. Endoscopy, also, demonstrated gastric polyps and duodenal polyposis. Endoscopical mucosal dyeing method using 0.2% methylene blue showed that the mucosal surface of the polyps was not dyed by methylene blue. Biopsy of the duodenal polyps revealed flat villi, cystic dilatation of the glands and stromal edema histologically.
View full abstract