A CASE REPORT OF GARDNER'S SYNDROME AND A REVIEW OF LITERATURE

Q: How can I download an article?

To download an article from SID, first log in to the site, search for the article title, and click on the 'Download Article' option.

Q: How can I download an ISI article?

To download an ISI article on SID, enter the keyword or article title in the search bar, view the relevant results, click on the desired article, and select the 'Download Article' option.

Q: How can I access the SID database?

To access the SID database, visit SID.ir, create an account, and log in to access scientific resources.

Q: Is downloading articles from SID free?

Some articles on SID are available for free, while others require payment. Details are specified on the article's page.

HEYDARPOUR MITRA; TABATABAEI S.A.; HEYDARPOUR MAJID; SAJADI F.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

Paper Information

Journal: IRANIAN JOURNAL OF PATHOLOGY (IJP) Year:2010 | Volume:5 | Issue:3 Page(s): 158-162

Download Full-Text

View:

316

Download:

112

Cites:

Information Journal Paper

Title

A CASE REPORT OF GARDNER'S SYNDROME AND A REVIEW OF LITERATURE

Author(s)

HEYDARPOUR MITRA | TABATABAEI S.A. | HEYDARPOUR MAJID | SAJADI F. | Issue Writer Certificate

Keywords

GARDNER’S SYNDROME

FAMILIAL POLYPOSIS COLI

ABDOMINAL FIBROMATOSIS

IRAN

Abstract

GARDNER’S SYNDROME is an autosomal dominant inherited disorder. Familial polyposis of the colon, osteomas, hypertrophy of the retinal-pigmented layer and a multitude of soft tissue tumors are characteristic features. The syndrome may be presented with colonic or extracolonic symptoms. A 75-year-old male patient presented to Al-zahra Clinic with diffuse abdominal pain. An abdominal surgery was performed on him due to invasive abdominal mass. The surgical specimen was examined by H&E and immunohistochemical staining. The final diagnosis was fibromatosis. There was a history of GARDNER’S SYNDROME in his family. Colonoscopy was done to confirm the diagnosis of GARDNER’S SYNDROME. The diagnosis of GARDNER’S SYNDROME was made according to following findings: ABDOMINAL FIBROMATOSIS, multiple jaw osteomas and polyposis coli. The patient with GARDNER’S SYNDROME can present with ABDOMINAL FIBROMATOSIS even in an old age. In IHC staining CD117 was seen with coarse granular cytoplasmic pattern in fibromatosis, and so, this pattern of CD117 staining can be a clue to the diagnosis of fibromatosis.

Cites

No record.

References

Cite

APA: Copy

HEYDARPOUR, MITRA, TABATABAEI, S.A., HEYDARPOUR, MAJID, & SAJADI, F.. (2010). A CASE REPORT OF GARDNER'S SYNDROME AND A REVIEW OF LITERATURE. IRANIAN JOURNAL OF PATHOLOGY (IJP), 5(3), 158-162. SID. https://sid.ir/paper/575988/en

Vancouver: Copy

HEYDARPOUR MITRA, TABATABAEI S.A., HEYDARPOUR MAJID, SAJADI F.. A CASE REPORT OF GARDNER'S SYNDROME AND A REVIEW OF LITERATURE. IRANIAN JOURNAL OF PATHOLOGY (IJP)[Internet]. 2010;5(3):158-162. Available from: https://sid.ir/paper/575988/en

IEEE: Copy

MITRA HEYDARPOUR, S.A. TABATABAEI, MAJID HEYDARPOUR, and F. SAJADI, “A CASE REPORT OF GARDNER'S SYNDROME AND A REVIEW OF LITERATURE,” IRANIAN JOURNAL OF PATHOLOGY (IJP), vol. 5, no. 3, pp. 158–162, 2010, [Online]. Available: https://sid.ir/paper/575988/en

Related Journal Papers

No record.

Related Seminar Papers

No record.

Related Plans

No record.

Recommended Workshops