Results of Surgery for a Compound Adrenal Tomor Consisting of Pheochromocytoma and Ganglioneuroblastoma in an Adult. 5-year Follow-up.
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- FUJIWARA Takuya
- the Second Department of Internal Medicine, Iwate Medical University
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- KAWAMURA Minoru
- the Second Department of Internal Medicine, Iwate Medical University
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- SASOU Shunichi
- the Department of Clinical Pathology, Iwate Medical University
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- HIRAMORI Katsuhiko
- the Second Department of Internal Medicine, Iwate Medical University
Bibliographic Information
- Other Title
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- Results of Surgery for a Compound Adrenal Tumor Consisting of Pheochromocytoma and Ganglioneuroblastoma in an Adult:5-year Follow-up
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Abstract
A rare, compound adrenal tumor consisting of ganglioneuroblastoma and pheochroniocytoma was completely resected in an adult woman. Most of the tumor was occupied by the ganglioneuroblastoma component. This ganglioneuroblastoma was an intermixed tumor, which is known to have a favorable prognosis in children. Based on the lack of spread, the resectability of the tumor, and the histology of the ganglioneuroblastoma, no adjuvant therapy was employed. There was no evidence of recurrence at the 5-year follow-up. This suggests that adjuvant therapy may not be necessary in these compound tumors.<br>(Internal Medicine 39: 58-62, 2000)
Journal
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- Internal Medicine
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Internal Medicine 39 (1), 58-62, 2000
The Japanese Society of Internal Medicine
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Details 詳細情報について
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- CRID
- 1390001204868423552
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- NII Article ID
- 10013261122
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- NII Book ID
- AA10827774
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- COI
- 1:STN:280:DC%2BD3c7jsleitA%3D%3D
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- ISSN
- 13497235
- 09182918
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- NDL BIB ID
- 4965432
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- PubMed
- 10674851
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- Text Lang
- en
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- Data Source
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- JaLC
- NDL
- Crossref
- PubMed
- CiNii Articles
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- Abstract License Flag
- Disallowed