Literature DB >> 18640357

Intrathoracic psammomatous melanotic schwannoma associated with the Carney complex.

Soeren Torge Mees1, Tilmann Spieker, Elke Eltze, Jens Brockmann, Norbert Senninger, Matthias Bruewer.   

Abstract

The Carney complex is a multiple neoplasia syndrome characterized by myxomas, schwannomas, mucocutaneous spotty pigmentations, and endocrine overactivity with or without endocrine tumors. Herein, we report the rare case of a 49-year-old man with a paravertebral intrathoracic tumor, a history of bilateral adrenalectomy, and resection of an atrial myxoma. A thoracoscopic en-bloc tumor extirpation with minimal safety margins was performed. Histopathologic examination revealed the diagnosis of a malignant psammomatous melanotic schwannoma that is associated with the Carney complex in 50% of these patients. Prognosis of all melanotic schwannomas is usually poor due to local recurrences or metastases. Although treatment guidelines for this rare tumor do not exist, radiotherapy was performed in our patient to prevent possible recurrence or regrowth of this malignant tumor. Twenty-four months after operation the patient showed no signs of tumor recurrence or metastases.

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Year:  2008        PMID: 18640357     DOI: 10.1016/j.athoracsur.2008.02.007

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  3 in total

1.  Novel response to neoadjuvant anti-PD1 therapy for a patient with retrocaval melanotic schwannoma.

Authors:  Charles C Vining; Phillip J Hsu; Aaron Miller; Daniel J Olson; Thomas F Gajewski; Peter Pytel; Bruce S Bauer; Michael J Millis; Kevin K Roggin
Journal:  Melanoma Res       Date:  2021-02-01       Impact factor: 3.199

2.  Post-operative Stereotactic Radiosurgery of Malignant Melanotic Schwannoma.

Authors:  Jennifer C Hall; Steven D Chang; Thomas J Wilson; Kristen N Ganjoo; Angus Toland; Hannes Vogel; Erqi L Pollom; Elham Rahimy
Journal:  Cureus       Date:  2022-03-04

3.  Non psammomatous melanocytic schwannoma presenting as a subcutaneous nodule: A rare presentation of a rare lesion.

Authors:  Harveen Kaur Gulati; Avinash R Joshi; Mani Anand; S D Deshmukh
Journal:  Asian J Neurosurg       Date:  2016 Jul-Sep
  3 in total

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