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A rare case of ganglioneuroblastoma encapsulated in pheochromocytoma
N. V. Sousa, L. C. Marques de Oliveira, P. J. Cortez, V. E. Valenti, D. M. Garner, R. de S. Irulegui, D. A. Moreira
Language English Country Czech Republic
Document type Case Reports, Journal Article
Digital library NLK
Full text - Article
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- MeSH
- 3-Iodobenzylguanidine MeSH
- Diagnosis, Differential MeSH
- Pheochromocytoma diagnostic imaging pathology MeSH
- Ganglioneuroblastoma diagnostic imaging pathology surgery MeSH
- Neoplasm Invasiveness MeSH
- Catecholamines urine MeSH
- Humans MeSH
- Magnetic Resonance Imaging * MeSH
- Neoplasms, Multiple Primary pathology MeSH
- Adrenal Glands diagnostic imaging pathology MeSH
- Adrenal Gland Neoplasms diagnostic imaging pathology MeSH
- Radionuclide Imaging MeSH
- Aged MeSH
- Rare Diseases * MeSH
- Check Tag
- Humans MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
Pheochromocytoma and Ganglioneuroblastoma are separate diseases and a rare combination in which the diagnosis can only be confirmed by pathological examination after tumor excision. We reported here a case of ganglioneuroblastoma encapsulated in pheochromocytoma. The patient is a woman, 73 years old, hypertensive, with hypothyroidism, associated for 15 years with hypercholesterolemia and hypertriglyceridemia, which had frequent complaints of low back pain. She underwent magnetic resonance and the findings were consistent with the diagnosis of pheochromocytoma. After surgery, anatomic, pathologic and immunohistochemistry analysis confirmed the diagnosis of pheochromocytoma composed by small ganglioneuroblastoma representation with the identification of small focus of infiltration of the adrenal capsule and adipose tissue by pheochromocytoma. This rare association can instigate the discussion of methods of diagnosis, more effective and more appropriate treatments for each patient.
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- $a Pheochromocytoma and Ganglioneuroblastoma are separate diseases and a rare combination in which the diagnosis can only be confirmed by pathological examination after tumor excision. We reported here a case of ganglioneuroblastoma encapsulated in pheochromocytoma. The patient is a woman, 73 years old, hypertensive, with hypothyroidism, associated for 15 years with hypercholesterolemia and hypertriglyceridemia, which had frequent complaints of low back pain. She underwent magnetic resonance and the findings were consistent with the diagnosis of pheochromocytoma. After surgery, anatomic, pathologic and immunohistochemistry analysis confirmed the diagnosis of pheochromocytoma composed by small ganglioneuroblastoma representation with the identification of small focus of infiltration of the adrenal capsule and adipose tissue by pheochromocytoma. This rare association can instigate the discussion of methods of diagnosis, more effective and more appropriate treatments for each patient.
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