| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5688613 | Urology | 2017 | 6 Pages |
Abstract
Paraganglioma (PGL) are rare tumors arising from extra-adrenal chromaffin cells and occasionally secret catecholamines. The patient commonly presents with headache, palpitation, anxiety, diaphoresis, and episodic or sustained hypertension. Rarely patient can present with Raynaud's phenomenon. We present a case of adolescent girl who presented with isolated Raynaud's phenomenon as only manifestation of metastasis of PGL 3 years after undergoing surgical excision of normetanephrine secreting abdominal PGL.
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Authors
Virendra Ashokrao Patil, Rajiv Kasaliwal, Manjunath R. Goroshi, Anurag R. Lila, Tushar Bandgar, Nalini S. Shah,