Median Nerve Parachordoma Masquerading Schwannoma: An Uncommon Case

Sumit Bansal, Pritinanda Mishra, Mamita Nayak, Rabi Sahu, Ashis Patnaik
2019 Indian Journal of Neurosurgery  
Benign tumors involving peripheral nerves of the upper extremity are uncommon. An entrapment syndrome resulting from the growing tumor causes symptoms. Pain is the most common complaint. We present a rare case of a median nerve parachordoma, a rare type of a benign tumor that presents as a palpable and painful mass on the flexor aspect of the forearm. A 62-year-old woman presented with a painful swelling at the flexor aspect of the right forearm. On clinical examination, there was a painful
more » ... e was a painful solid mass, which was 2 cm in length, little sensitive to pressure, and had mobility restriction in both transverse and longitudinal directions. Percussion over the mass produced a Tinel's-like sensation along the median nerve. The patient experienced mild numbness in the distribution of the median nerve in the palm, but no motor weakness or muscle atrophy was noticed. On magnetic resonance imaging (MRI) examination, lesion had a relatively homogenous low signal, slightly lower to the flexor tendon of the forearm, on T1-weighted images. On T1 fat-suppressed contrast images, increased gadolinium enhancement was noticed (►Fig. 1a, b) . Based on the clinical and MRI features, provisional diagnosis of a nerve sheath tumor arising from the median nerve was made. A longitudinal incision centered over the tumor bulk at the distal part of flexor aspect of right forearm was performed. Adequate exposure of the nerve was done, both proximal and distal to the tumor. On exploration, the tumor was found to arise from the median nerve in the right forearm, below the flexor tendon. The tumor had an eccentric position and was firmly attached to the median nerve. The epineurium was longitudinally incised, and the soft tumor mass was dissected from surrounding nerve fascicles. The mass was encapsulated and removed completely (►Fig. 1c, d). Postoperative course was uneventful with no new neurologic deficit. The histopathology report was suggestive of parachordoma (►Fig. 2). At 1-month follow-up, the wound was healed with no new symptoms. Parachordomas (or myoepitheliomas) are rare soft tissue tumors with approximately 100 cases reported, 1 with Indian J Neurosurg 2019;8:145-146 Fig. 1 MRI examination of right forearm showed contrast-enhancing lesion deep to the flexor tendon of forearm (a, b) . The tumor was arising from the median nerve in the right forearm, below the flexor tendon of forearm (c). The mass was encapsulated and removed totally (d). Fig. 2 (a) Epithelioid cells and spindle cells lying in myxoid stroma (H&E 100X). (b) Epithelioid cells with clear cytoplasm (H&E 400X). (c-e) Tumor cells are immunopositive for S-100, cytokeratin, and negative for P53 (IHC 400X).
doi:10.1055/s-0039-1694840 fatcat:2555f6uomzckdbwwryexnbhn4u