Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 1992 Oct;37(10):1624-9.
doi: 10.1007/BF01296512.

Heterotopic bone formation in rectal carcinoma. Case report and literature review

Affiliations
Review

Heterotopic bone formation in rectal carcinoma. Case report and literature review

M Q Ansari et al. Dig Dis Sci. 1992 Oct.

Abstract

A case of heterotopic bone formation in a primary rectal adenocarcinoma was recently observed in a 54-year-old woman. This unusual finding was present both in the diagnostic biopsy and in the subsequently resected bowel. Pertinent gross and microscopic features are presented. This report represents the twelfth case in the literature of heterotopic bone formation in a primary rectal adenocarcinoma and the first such finding in a colonic biopsy from one of these malignancies. The average age of these patients was 56 years (range 32-72) and the male-to-female ratio was 5:7. The rectum is the most common site of ossification in the gastrointestinal tract. The exact mechanism of heterotopic ossification is unknown, but it is probably the result of metaplasia of fibroblasts. Adenocarcinoma has been associated with 12 of the 16 reported cases of rectal glandular tumors with heterotopic bone.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Lab Invest. 1989 Mar;60(3):320-30 - PubMed
    1. Z Krebsforsch Klin Onkol Cancer Res Clin Oncol. 1976 Jun 15;86(2):147-54 - PubMed
    1. Am J Surg. 1972 Jul;124(1):108-11 - PubMed
    1. Proc R Soc Med. 1939 Sep;32(11):1489-94 - PubMed
    1. JAMA. 1962 Feb 3;179:347-50 - PubMed