Osseous Metaplasia in A Juvenile Polyp: A Rare Case Report in India

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Osseous metaplasia in a juvenile polyp: a rare case report in India.

Osseous metaplasia is a phenomenon which is described in a variety of tissue types with respect to both neoplastic and non-neoplastic conditions. In the gastrointestinal tract, osseous metaplasia (heterotopic bone formation) is rarely detected. Most of the reported cases were associated with malignant lesions. Here, we are reporting a rare case of a juvenile rectal polyp in a 14 years male, whi...

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Septochoanal polyp with osseous metaplasia: a case report

BACKGROUND Polyps originating from the posterior septum with choanal extension, also known as "septochoanal polyps," are uncommon, and septochoanal polyps with central calcification are extremely rare. We report the second case of septochoanal polyps with central calcification in the English literature. CASE PRESENTATION A 55-year-old Thai woman presented with a progressive left-side nasal ob...

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Osseous metaplasia in a gastric adenomatous polyp.

Heterotopic bone is rarely found in the gastrointestinal tract. In the majority of reported cases, it was associatedwith malignant lesions [1,2], Peutz–Jeghers syndrome [3], and more rarely with inflammatory colonic polyps [4]. On reviewing the literature, we found only two cases of metaplastic bone accompanying hyperplastic gastric mucosa [5,6], and no case report of osseous metaplasia in gast...

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[Endometrial osseous metaplasia: A case report].

Endometrial osseous metaplasia (EOM) is a rare condition characterised by the presence of bone in the uterine cavity. Some patients with this condition present with secondary infertility due to the presence of a foreign body in the endometrium. We report a case of a 39-year-old woman who presented with secondary infertility due to EOM. EOM is a rare cause of infertility that can be easily manag...

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Posterior Urethral Polyp: A Rare Case

Urethral polyps are a rare finding in children. Urethral fibroepithelial polyps are usually discovered in the first decade of life. They present with voiding dysfunction, obstructive and irritative urinary symptoms, and hematuria. They may be associated with other congenital urinary tract anomalies. Histopathologically, they are usually benign lesions with no tendency to recurrence and are trea...

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ژورنال

عنوان ژورنال: JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH

سال: 2013

ISSN: 2249-782X

DOI: 10.7860/jcdr/2013/5789.3385