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Reviewing Schwannoma-Hemangioma Composite Tumors With Their Tumorigenetic Molecular Pathways and Associated Syndromic Manifestations

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CUREUS JOURNAL OF MEDICAL SCIENCE
卷 13, 期 11, 页码 -

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SPRINGERNATURE
DOI: 10.7759/cureus.19839

关键词

hemangioma; merlin; vegf; tie 2; angiopoitein; hamartin; tuberin; tuberous sclerosis; schwannoma

资金

  1. PathnSitu Biotechnologies, Hyderabad, Telangana, India
  2. PathnSitu Biotechnologies, Pleasanton, CA, USA

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Schwannomas and neurofibromas are the most prevalent tumors associated with cavernous hemangiomas, with only 37 documented cases of their coexistence so far. These cases are divided into conjoined association and discrete association categories, with implications for tumorigenetic molecular pathways and syndromic manifestations emphasized in previous publications.
Schwannomas are common peripheral nerve sheath tumors. Cavernous hemangiomas are vascular tumors that can affect any organ system. The coexistence of cavernous hemangioma with peripheral nervous system neoplasms is a rare occurrence. So far, 37 cases have been documented, and they have been divided into two categories: conjoined association (neoplasms discovered within the tumor tissue) and discrete association (neoplasms discovered outside the tumor tissue, thus placing neoplasms and tumors in close proximity but in different locations). Schwannomas and neurofibromas are the most prevalent tumors linked to cavernous hemangiomas that have been documented. The author provides a comprehensive review of all such cases published in the past with an emphasis on the implications of their tumorigenetic molecular pathways and syndromic manifestations.

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