Results 121 to 130 of about 2,191 (165)
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The Journal of Laryngology & Otology, 1991
AbstractA 41-year-old male Egyptian patient presented with difficulty in swallowing, snoring, and the sensation of a lump in his throat over a long period of time. On examination, a left tonsillar polyp was seen ( 4 × 2 × 1 cm) which was pedunculated, bilobulate, with an intact surface.
K A, Shara +2 more
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AbstractA 41-year-old male Egyptian patient presented with difficulty in swallowing, snoring, and the sensation of a lump in his throat over a long period of time. On examination, a left tonsillar polyp was seen ( 4 × 2 × 1 cm) which was pedunculated, bilobulate, with an intact surface.
K A, Shara +2 more
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Hamartomatous Polyp of the Hypopharynx
Acta Otorrinolaringologica (English Edition), 2011We present the clinical case of a polyp in the hypopharynx discovered incidentally while performing an upper digestive endoscopy in a middle aged woman. Endoscopic resection was performed, and the histological result was a hamartomatous polyp. We review the diagnosis and treatment of this rare entity.
Teresa, Millás-Gómez +4 more
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Hamartomatous Polyp of the Esophagus
Archives of Surgery, 1975Hamartomatous polyp of the cervical esophagus in a 60-year-old man was treated by local resection, and the patient did well. The histopathologic findings showed a predominance of cartilaginous tissue, but the specimen also contained glandular structures and adipose tissue. The diagnosis was choristoma or hamartoma.
B, Shah, L, Unger, H J, Heimlich
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Management of Hamartomatous Polyps
2020Hamartomatous polyps may arise as solitary lesions, usually in childhood or early adolescence and, are denoted histologically by an overgrowth of mesenchymal or ectodermal cell native to the area of origin. These polyps may occur “sporadically” or in the context of inherited syndromes.
Peter C. Ambe, Gabriela Möslein
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Hamartomatous Polyp of Brunner's Glands
Gastroenterology, 1963Summary Twenty-five cases of pathologic proliferation of Brunner's glands reported in the English literature are reviewed and another case is described. Symptoms are nonspecific and may imitate more common upper gastrointestinal disease entities.
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Benign hamartomatous polyp of the palatine tonsil
The Journal of Laryngology & Otology, 1993AbstractA rare and possibly unique benign polypoid tumour of the palatine tonsil is described. It contained the two basic tissue types of the tonsil–lymphoid and epithelial–in the characteristic close anatomical relationship of tonsillar tissue. The features of this rare lesion lend support to the hypothesis that benign tumours of the tonsil may be ...
A, Lupovitch +2 more
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Hamartomatous Polyps in the Intestine of Two Dogs
Journal of Comparative Pathology, 1994Partly obstructing, proliferative mucosal masses in the small intestine of two dogs were shown histologically to be hamartomatous polyps. They were characterized by an extension of smooth muscle from the muscularis mucosae into the lamina propria of the lesion. This is the first report of such lesions in domestic animals.
P J, Brown +4 more
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Hamartomatous Polyp of the Tonsil: A Case Report
Nigerian Journal of Clinical Practice, 2017Hamartomatous polyps of the tonsil are rare. They have been described using various terms such as a lymphangiomatous polyp, lymphangiectatic fibrous polyp, lipomatous polyp, or pedunculated tonsil; hence, the actual incidence is difficult to be quantified. Polyp of the palatine tonsils is an unusual benign lesion of the head and neck.
Singh, M, Mundi, D.K., Kaur, I, Kaur, A
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Hamartomatous inverted polyps of the rectum
Cancer, 1966Hamartomatous inverted polyps of the rectum are benign single slightly polypoid intramural masses of the bowel wall formed by an inverted or downward growth of mucosal glands through the muscularis mucosa into the submucosa. The atypical and distorted mucous glands and the ectopic position of both mucous glands and lakes of mucus in these benign ...
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Hamartomatous Polyp of the Gallbladder With an Associated Choledochal Cyst
Journal of Ultrasound in Medicine, 2010A hamartomatous polyp is an extremely rare polypoidal lesion of the gallbladder, with the first case having been reported in 1998. 1 To the best of our knowledge, fewer than 10 hamartomatous gallbladder polyps have been reported in patients with Peutz-Jeghers syndrome (PJS).
A Devrim, Karaosmanoglu, Michael, Blake
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