Literature DB >> 17199864

Two von Recklinghausen's disease cases with pheochromocytomas and gastrointestinal stromal tumors (GIST) in combination.

Sakiko Teramoto1, Tomonori Ota, Akimitsu Maniwa, Takashi Matsui, Naoshi Itaya, Kazumi Aoyagi, Hiroshi Kusanagi, Makoto Narita.   

Abstract

We here document two cases of von Recklinghausen's disease with both pheochromocytomas and gastrointestinal stromal tumors (GIST). It is very rare that these three disorders are found to occur simultaneously, although the fact that preoperative detection of GIST is difficult except with large tumors may be important in this respect. In the present cases, GIST were not evident on preoperative computed tomography and magnetic resonance imaging, and were identified unexpectedly during surgery. Our findings indicate that investigation of the intraperitoneal space should be performed during adrenalectomy for pheochromocytomas with von Recklinghausen's disease.

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Year:  2007        PMID: 17199864     DOI: 10.1111/j.1442-2042.2006.01601.x

Source DB:  PubMed          Journal:  Int J Urol        ISSN: 0919-8172            Impact factor:   3.369


  11 in total

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5.  Neurofibromatosis type 1 associated with pheochromocytoma and gastrointestinal stromal tumors: A case report and literature review.

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6.  Multiple gastrointestinal stromal tumors and pheochromocytoma in a patient with von Recklinghausen's disease.

Authors:  Beyza Ozcinar; Nihat Aksakal; Orhan Agcaoglu; Mustafa Tukenmez; Ibrahim A Ozemir; Umut Barbaros; Nese Colak; Yesim Erbil
Journal:  Int J Surg Case Rep       Date:  2012-11-23

7.  c-KIT positive Gastrointestinal Stromal Tumor presenting with acute bleeding in a patient with neurofibromatosis type 1: a case report.

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8.  Use of balloon enteroscopy in preoperative diagnosis of neurofibromatosis-associated gastrointestinal stromal tumours of the small bowel: a case report.

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9.  Pancreatic insulinoma co-existing with gastric GIST in the absence of neurofibromatosis-1.

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Review 10.  Pheochromocytoma and gastrointestinal stromal tumours in an adult neurofibromatosis type 1 patient: a rare co-occurrence.

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Journal:  BMJ Case Rep       Date:  2020-06-28
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