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1. www.slideshare.net › GAMANDEEP › pheochromocytoma-144103879Pheochromocytoma | PPT - SlideShare

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   2019年5月7日 · Pheochromocytoma | PPT. May 7, 2019 •. 97 likes • 42,751 views. GAMANDEEP. Pheochromocytoma with nursing management. Healthcare. Slideshow view. Pheochromocytoma - Download as a PDF or view online for free.

2. www.slideshare.net › slideshow › pheochromocytoma-84925382Pheochromocytoma | PPT - SlideShare

   www.slideshare.net › slideshow › pheochromocytoma-84925382

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   2017年12月25日 · Phreochromocytoma : overvew, introduction, adrenal gland anatomy and physiology, adrenl gland tumor classification, epidemiology, clinical features, investigations. Read more. Healthcare. Download now. Pheochromocytoma - Download as a PDF or view online for free.

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     Pheochromocytoma | Symptoms and Treatment

     2019年2月17日

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     PPT - Pheochromocytoma PowerPoint Presentation, free download - ID:6451003

     2014年11月25日

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     slideserve.com

     PPT - Pheochromocytoma PowerPoint Presentation, free download - ID:4276183

     2019年3月29日

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4. www.slideshare.net › slideshow › pheochromocytoma-51486172Pheochromocytoma | PPT - SlideShare

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   2015年8月11日 · Pheochromocytoma is a catecholamine-producing tumor that arises from chromaffin cells of the sympathetic nervous system. It occurs in about 0.1-0.2% of hypertensive patients and can cause paroxysmal or sustained hypertension. Diagnosis involves measuring catecholamines or metanephrines in plasma or urine, which are elevated in most patients.

5. www.uptodate.com › contents › clinical-presentation-andClinical presentation and diagnosis of pheochromocytoma

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   2024年5月9日 · The clinical presentation and approach to diagnosis of pheochromocytoma are reviewed here. The genetics and treatment of pheochromocytoma and the clinical manifestations, diagnosis, and treatment of paragangliomas are discussed separately.

6. emedicine.medscape.com › article › 124059-clinicalPheochromocytoma Clinical Presentation: History, Physical ...

   emedicine.medscape.com › article › 124059-clinical

   2024年4月26日 · Pheochromocytoma Clinical Presentation. Updated: Apr 26, 2024. Author: Michael A Blake, MBBCh, MRCPI, FRCR; Chief Editor: George T Griffing, MD more... Print. History. Symptoms and signs of...

7. 其他人也問了

   What are pheochromocytomas?

   • Pheochromocytomas are tumors arising from chromaffin cells of the adrenal medulla. The clinical manifestations of these tumors are primarily related to the excessive secretion of catecholamines. Similar tumors that arise from extra-adrenal chromaffin cells have been referred to as paragangliomas.

   Pheochromocytoma - StatPearls - NCBI Bookshelf

   www.ncbi.nlm.nih.gov/books/NBK589700/

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   What are the signs and symptoms of pheochromocytoma?

   • Symptoms and signs of pheochromocytoma include the following: The classic history of a patient with a pheochromocytoma includes spells characterized by headaches, palpitations, and diaphoresis in association with severe hypertension. These 4 characteristics together are strongly suggestive of a pheochromocytoma.

   Pheochromocytoma Clinical Presentation - Medscape

   emedicine.medscape.com/article/124059-clinical

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   What does a pheochromocytoma look like?

   • The classic history of a patient with a pheochromocytoma includes spells characterized by headaches, palpitations, and diaphoresis in association with severe hypertension. These 4 characteristics together are strongly suggestive of a pheochromocytoma. In the absence of these 3 symptoms and hypertension, the diagnosis may be excluded.

   Pheochromocytoma Clinical Presentation - Medscape

   emedicine.medscape.com/article/124059-clinical

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   Do pheochromocytomas recur?

   • It is essential to recognize the risk of recurrence of pheochromocytomas. This risk is present in sporadic as well as familial cases. In a study of 192 patients with pheochromocytomas and paragangliomas, the recurrence risk was higher in familial, right adrenal, and extra-adrenal tumors.

   Pheochromocytoma - StatPearls - NCBI Bookshelf

   www.ncbi.nlm.nih.gov/books/NBK589700/

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8. www.ncbi.nlm.nih.gov › books › NBK589700Pheochromocytoma - StatPearls - NCBI Bookshelf

   www.ncbi.nlm.nih.gov › books › NBK589700

   2023年3月5日 · Pheochromocytomas are tumors arising from chromaffin cells of the adrenal medulla. The clinical manifestations of these tumors are primarily related to the excessive secretion of catecholamines. Similar tumors that arise from extra-adrenal chromaffin cells have been referred to as paragangliomas. [1]

9. pubmed.ncbi.nlm.nih.gov › 17082709Pheochromocytoma: presentation, diagnosis and treatment

   pubmed.ncbi.nlm.nih.gov › 17082709

   Pheochromocytomas are rare, mostly benign catecholamine-producing tumors of chromaffin cells of the adrenal medulla or of a paraganglion. Typical clinical manifestations are sustained or paroxysmal hypertension, severe headaches, palpitations and sweating resulting from hormone excess.