التفاصيل البيبلوغرافية
| العنوان: |
A rare combination of pheochromocytoma and gastrointestinal stromal tumour in a patient with neurofibromatosis 1 syndrome—a case report |
| المؤلفون: |
Jayalakshmy, P S, Mohan, A., Kumar, Rajesk, Beevi, P. |
| بيانات النشر: |
BioMed Central Ltd. |
| سنة النشر: |
2015 |
| المجموعة: |
BioMed Central |
| مصطلحات موضوعية: |
Brown fat, Clear cell nodules, Gastrointestinal stromal tumour (GIST), Inherited syndromes, Neurofibromatosis 1 (NF1), Pheochromocytoma |
| الوصف: |
Neurofibromatosis 1 is a rare inherited autosomal dominant syndrome. It comprises 90 % of neurofibromatosis cases. These patients may develop various types of tumours in early age, especially multiple neurofibromas with a high risk of developing malignant peripheral nerve sheath tumours. Other tumours can also develop like pheochromocytoma, optic nerve and brain stem gliomas, carcinoids and rarely gastrointestinal stromal tumours. A combination of pheochromocytoma and gastrointestinal stromal tumour is very rare. Only a few cases have been reported. Here, we are reporting a case of NF1 syndrome with a combination of pheochromocytoma and gastrointestinal stromal tumour with additional findings of multiple clear cell nodules and brown fat in the periadrenal connective tissue. |
| نوع الوثيقة: |
report |
| اللغة: |
English |
| العلاقة: |
http://www.surgicalcasereports.com/content/1/1/102Test |
| الإتاحة: |
http://www.surgicalcasereports.com/content/1/1/102Test |
| حقوق: |
Copyright 2015 Jayalakshmy et al. |
| رقم الانضمام: |
edsbas.96B1D81B |
| قاعدة البيانات: |
BASE |
