Three cases of intestinal polyposis in a family.
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Heredity↗
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Results for “Intestinal Polyposis”
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Sotos syndrome with intestinal polyposis and pigmentary changes of the genitalia.
We report two adult males with the Sotos syndrome, who also presented intestinal polyposis and pigmentary spotting of the shaft and glans penis. We propose that patients with the Sotos syndrome may develop hamartoneoplastic disease and we urge clinicians to consider this possibility in those patients.
Abnormalities, Multiple↗
[Intestinal polyposis with mucocutaneous pigmentation].
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Humans↗
Melanin spots of the lips, oral mucosa and digits associated with intestinal polyposis; report of a case.
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Humans↗
[Intestinal polyposis with peri-orificial lentiginosis; Peutz syndrome].
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Intestinal Neoplasms↗
Genetic factors in hereditary intestinal polyposis and oral pigmentation.
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Humans↗
Hereditary intestinal polyposis with oral pigmentation (Jeghers' syndrome); a case report.
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Intestinal Neoplasms↗
Surface pigmentation and generalized intestinal polyposis; (Peutz-Jeghers syndrome).
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Intestinal Neoplasms↗
[Generalized intestinal polyposis. Peutz-Jeghers syndrome. Gardner syndrome].
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Gardner Syndrome↗
Intestinal polyposis and periampullary carcinoma--changing concepts.
Adenomatous polyps lead directly to carcinoma of the colon in patients with one of the familial syndromes of intestinal polyposis. Elective colectomy is prophylactic and life-saving. A subgroup of patients will develop periampullary carcinoma, again arising from the presence of adenomatous polyps. Such a case is presented. These polyps should be surgically excised to ensure adequate pathologic examination. Yearly upper endoscopic examination is an essential element of management. Either the presence of carcinoma in situ or the recurrence of these polyps following excision is confirmation of behavior with a high propensity for the development of invasive cancer and requires aggressive treatment.
Adenocarcinoma↗
Intestinal polyposis.
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Intestinal Neoplasms↗
Carcinoma of jejunum in intestinal polyposis with oral and digital melanosis.
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Intestinal Polyposis↗
Intestinal polyposis associated with mucocutaneous pigmentation.
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Humans↗
Hereditary small intestinal polyposis with intussusception and oral pigmentation in two generations: Peutz-Jeghers syndrome.
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Humans↗
Intestinal polyposis associated with mucocutaneous pigmentation.
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Intestinal Neoplasms↗
Intestinal polyposis and carcinoma originating from a mutation in a family group.
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Humans↗
Genetic factors in intestinal polyposis.
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Genetics, Medical↗
Intestinal polyposis associated with pigmentation of the lips, buccal mucosa and digits.
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Disease↗