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Indian Journal of Pathology and Microbiology
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CASE REPORT
Year : 2018  |  Volume : 61  |  Issue : 3  |  Page : 404-406

Paraganglioma with a very rare presentation


1 Department of Pathology, JNUIMSRC, Jaipur, Rajasthan, India
2 Department of Surgery, JNUIMSRC, Jaipur, Rajasthan, India

Correspondence Address:
Manika Khare
Department of Pathology, JNUIMSRC, Jaipur, Rajasthan
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/IJPM.IJPM_334_17

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Paragangliomas (PGLs) are rare tumors of neural crest origin, with a malignancy rate of approximately 10% and a 5-year survival rate of <50%. We present a case of malignant PGL arising from the porta hepatis with metastasis to the portal lymph node and bilateral ovaries. PGLs arising from the porta hepatis are very rare. As per our knowledge, only three cases of hepatic duct PGL have been reported. It is important to detect it earlier because the treatment modality and prognosis of benign and malignant PGL differs and defines the prognosis of the patient.


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