Mediastinal Primitive Neuroectodermal Tumour (PNET) – A Rare Case of Horner’s Syndrome

Authors

  • Anirban Das Assistant Professor, Department of Pulmonary Medicine, Medical College, Kolkata.
  • Partha Pratim Roy Professor& H.O.D, Pulmonary Medicine, Medical College, Kolkata.
  • Anirban Sarkar MD (TB & Respiratory Medicine); Assistant Professor, Department of Pulmonary Medicine, Medical College, Kolkata.
  • Samadarshi Datta RMO?cum?Clinical Tutor, Department of Pulmonary Medicine, Medical College, Kolkata.
  • Subir Dey Professor, Department of Pulmonary Medicine, Calcutta National Medical College, Kolkata.
  • Nandita Basu Professor& HOD, Pathology, Midnapore Medical College, Midnapore.

DOI:

https://doi.org/10.3329/jom.v13i1.8762

Keywords:

Primitive neuroectodermal tumour (PNET), Mediastinal tumour, Horner’s syndrome, Superior vena caval onbstruction, Round cell tumour, CD – 99

Abstract

Primitive neuroectodermal tumour (PNET) is a rare mediastinal tumour which may infiltrate pulmonary parenchyma and chest wall. Histopathologically, it is a round cell tumour, and on immunohistochemistry, tumour cells express for CD – 99 (MIC – 2). Here we report a rare case of PNET presented as unresectable mediastinal tumour with chest wall infiltration, superior vena caval obstruction and Horner’s syndrome in an adolescent female.

DOI: http://dx.doi.org/10.3329/jom.v13i1.8762

JOM 2012; 13(1): 85-87

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Published

2012-03-12

How to Cite

Das, A., Roy, P. P., Sarkar, A., Datta, S., Dey, S., & Basu, N. (2012). Mediastinal Primitive Neuroectodermal Tumour (PNET) – A Rare Case of Horner’s Syndrome. Journal of Medicine, 13(1), 85–87. https://doi.org/10.3329/jom.v13i1.8762

Issue

Vol. 13 No. 1 (2012)

Section

Case Reports

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