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epidermal cyst/diarrhée
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Epidermoid cyst of the ileum in a miniature dachshund dog.
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A 13-year-old castrated male miniature dachshund dog was presented with chronic vomiting and diarrhea. Contrast radiography and surgical exploration revealed an ileal cyst, which was excised. A diagnosis of epidermoid cyst was made from a combination of the clinical findings and histological
Meningitis complicating an occult infected nasal epidermoid cyst in a child.
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Congenital nasal epidermoid cyst without associated facial dysmorphism is an uncommon anomaly that is often asymptomatic. We report a case of occult nasal epidermoid cyst in a 12-year-old boy with initial nonspecific symptoms of fever, headache, abdominal pain, vomiting, and diarrhea. An enhanced
A rapidly growing epidermoid cyst in an intrapancreatic accessory spleen treated by laparoscopic spleen-preserving distal pancreatectomy: Report of a case.
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Epidermoid cysts arising in an intrapancreatic accessory spleen are exceedingly rare, furthermore the natural course of them is hardly known. We report a case correctly diagnosed with epidermoid cyst in an intrapancreatic accessory spleen, followed by 1 year observation, finally underwent surgical
[Clinical investigation of a long-acting amoxicillin preparation in patients with skin and soft-tissue infections].
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A clinical investigation of a long-acting amoxicillin preparation (L-AMPC) in 82 patients (81 with skin and soft-tissue infections and 1 with osteomyelitis) gave the following results. Staphylococcus aureus and Staphylococcus epidermidis were most frequently detected organisms. With an inoculum of
Familial polyposis coli: clinical manifestations, evaluation, management and treatment.
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Familial adenomatous polyposis (FAP) is an autosomal dominant, hereditary colon cancer syndrome that is characterized by the presence of innumerable adenomatous polyps in the colon and rectum. Gardner's syndrome is a variant of FAP, which in addition to the colonic polyps, also presents extracolonic
Primary carcinoid tumors of the testis: a clinicopathologic study of 29 cases.
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Testicular carcinoid tumors are rare with only limited studies. We identified 29 primary testicular carcinoid cases from 7 academic institutions. Patients ranged in age from 12 to 65 years old (mean 36). The most common presenting symptom was the sole finding of either a testicular mass or swelling
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