Title: Composite Pheochromocytoma- A Case Report

Authors: P. Divya, M. Mounika, S.Sharath Chandran, B. Krishnaswamy, Rehana Tippoo, P. Viswanathan

 DOI: https://dx.doi.org/10.18535/jmscr/v7i5.14

Abstract

Pheochromocytoma originates from primitive neuroectodermal cell rest in adrenals and other paraganglion structures. The term composite pheochromocytoma is used in reference to pheochromocytoma where there are other components resembling neuroblastoma, ganglioneuroblastoma, ganglioneuroma and spindle cell sarcomatous tumour coexist. Here a 61 year old man with pheochromocytoma of right adrenal gland along with tumour component of MPNST-malignant peripheral nerve sheath tumour co-exist  (Composite pheochromocytoma) is being presented. The patient presented with left flank pain of one month duration along with complaints of Insomnia, anxiety, palpitation and persistent constipation of short duration.

Keywords: Pheochromocytoma, Composite Pheochromocytoma, Adrenal gland tumor.

References

  1. Ernest E. Lack, Tumors of the adrenal glands & extra adrenal Paraganglia. AFIP atlas of tumor pathology series 4.2009,241-260.
  2. Christopher D.M. Fletcher, Diagnostic Histopathology of Tumors, 4th edition, volume 1,1307-1314.
  3. Weidner, Cote, Suster, Weiss, Modern Surgical Pathology, volume 2,1765-1772.
  4. Shawa H, Elsayes KM, Jawadi S, Sircar K, Jimenez C, Habra MA. Clinical and radiological featuires of pheochrmocytoma / ganglioneuroma composite tumours: a case series with comparative analysis. Endocr Pract.2014;20:864-869.
  5. Rao RN, Singla N, Yadav K. Composite pheochromocytoma-ganglio neuroma of the adrenal gland: A case report with Immuno histochemical study. Urology Annals. 2013; 5: 115-118.

Corresponding Author

P Viswanathan

Professor in Pathology, Department of Pathology, Rajah Muthiah Medical College and Hospital, Annamalai University, Annamalainagar, Chidambaram- 608002

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