HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS		QUICK SEARCH:   [advanced] Author: Keyword(s): Year:  Vol:  Page:

This Article Figures Only Full Text Full Text (PDF) CME Test (opens in a new window) Submit a response Alert me when this article is cited Alert me when eLetters are posted Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Levy, A. D. Articles by Sobin, L. H. Search for Related Content PubMed PubMed Citation Articles by Levy, A. D. Articles by Sobin, L. H. Related Collections Gastrointestinal Radiology

From the Archives of the AFIP

Abdominal Neoplasms in Patients with Neurofibromatosis Type 1: Radiologic-Pathologic Correlation¹

¹ From the Departments of Radiologic Pathology (A.D.L., R.M.A.), Hepatic and Gastrointestinal Pathology (N.D., L.H.S), and Soft Tissue Pathology (M.M.), Armed Forces Institute of Pathology, Alaska and Fern Sts NW, Washington, DC 20306-6000; Department of Medical Education, Washington Hospital Center, Washington, DC (N.P.); Department of Radiology, University of Maryland School of Medicine, Baltimore (R.M.A.); and Department of Radiology and Nuclear Medicine, Uniformed Services University of the Health Sciences, Bethesda, Md (A.D.L., R.M.A.). Received September 1, 2004; accepted September 20. All authors have no financial relationships to disclose. Address correspondence to A.D.L. (e-mail: levya{at}afip.osd.mil).

Neurofibromatosis type 1 (NF1) is one of the most common genetic disorders. NF1 is a complex disease resulting from a spectrum of mutations that may occur at many locations along the large, complex NF1 gene, which is located on chromosome 17. Mutations of the NF1 gene lead to abnormal tumor suppression. Consequently, patients with NF1 have an increased prevalence of benign and malignant neoplasms throughout the body. There are five categories of NF1 tumors that occur in the abdomen: neurogenic, neuroendocrine, nonneurogenic gastrointestinal mesenchymal, embryonal, and miscellaneous. Many of these tumors are age related, occur at specific anatomic locations, and have unique imaging features. Notably, many patients have a variety of organs affected because there is a high prevalence of multiple tumors occurring in the same patient. Neurofibromas are the most common benign neoplasms and may occur in the retroperitoneum or visceral organs. Malignant peripheral nerve sheath tumor is an aggressive malignancy that is the most common malignant tumor of the abdomen in patients with NF1. Interpreting abdominal imaging studies in patients with NF1 can be challenging because of the wide spectrum and diverse nature of tumors that occur in this disease.

Abbreviations: H-E = hematoxylin-eosin, MPNST = malignant peripheral nerve sheath tumor, NF1 = neurofibromatosis type 1

This article has been cited by other articles:

				S W KIM, H C SHIN, I Y KIM, K-H KANG, and H-D CHO Multiple gastrointestinal stromal tumours presenting as a haemoperitoneum in a patient with Type 1 neurofibromatosis: MDCT findings Br. J. Radiol., July 1, 2009; 82(979): e133 - e136. [Abstract] [Full Text] [PDF]

				G Gokalp, B Hakyemez, E Kizilkaya, and A Haholu Myxoid neurofibromas of the breast: mammographical, sonographical and MRI appearances Br. J. Radiol., October 1, 2007; 80(958): e234 - e237. [Abstract] [Full Text] [PDF]

				J. J. Wong-You-Cheong, P. J. Woodward, M. A. Manning, and I. A. Sesterhenn From the Archives of the AFIP: Neoplasms of the Urinary Bladder: Radiologic-Pathologic Correlation RadioGraphics, March 1, 2006; 26(2): 553 - 580. [Abstract] [Full Text] [PDF]