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Primary intracranial malignant melanomas in solitary type: a tertiary center experience.
Huang, Yen-Min; Yeh, Kun-Yun; Chen, Pin-Yuan; Hsieh, Tsan-Yu; Hsu, Li-Sung; Wu, Chiao-En; Yang, Cheng-Han; Zheng, Yun-Cong.
Afiliação
  • Huang YM; Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Keelung, Taiwan; Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan. Electronic address: 8902004@cgmh.org.tw.
  • Yeh KY; Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Keelung, Taiwan. Electronic address: yehtyng@gmail.com.
  • Chen PY; Departments of Neurosurgery, Chang Gung Memorial Hospital, Keelung and Linkou & Chang Gung University, Taiwan. Electronic address: pinyuanc@cgmh.org.tw.
  • Hsieh TY; Department of Pathology, Chang Gung Memorial Hospital, Keelung, Taiwan. Electronic address: b8902059@gmail.com.
  • Hsu LS; Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan. Electronic address: hym1000.tw@yahoo.com.tw.
  • Wu CE; Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan. Electronic address: jiaoen@gmail.com.
  • Yang CH; Departments of Anatomic Pathology, Chang Gung Memorial Hospital at Linkou. Electronic address: chuckchy@gmail.com.
  • Zheng YC; Departments of Neurosurgery, Chang Gung Memorial Hospital, Keelung and Linkou & Chang Gung University, Taiwan. Electronic address: m7630@cgmh.org.tw.
J Clin Neurosci ; 101: 37-46, 2022 Jul.
Article em En | MEDLINE | ID: mdl-35526362
ABSTRACT

PURPOSE:

Solitary type primary intracranial malignant melanoma (PIMM) is extremely rare but fatal. The optimal treatment algorithm according to clinical relevance of symptoms and outcomes is unclear. This series emphasized the prognostic factors of solitary PIMM and established the treatment algorithm for this rare disease.

METHODS:

Patients with solitary PIMMs were pathologically verified and treated with neurosurgical tumor resection. All solitary PIMMs recruited at our institute received multidisciplinary team care. We analyzed the clinical findings and prognostic factors.

RESULTS:

The study cohort included 10 patients. PIMMs in solitary type impacted middle-aged populations with male predominance in Taiwan. Most patients (80%) presented a single tumor initially. Six patients had progressed to multiplicity after the initial treatment. Rates of tumor bleeding and leptomeningeal metastasis seeding (LS) are high in solitary PIMMs. Patients who had gross-total resection (GTR) had better survival than those who had incomplete resection, with median overall survival (OS) rates of 170.4 months vs. 5.23 months (p = 0.004). Multiplicity, eloquent area involvement, initial tumor bleeding, LS, hydrocephalus, and Karnofsky Performance Score < 80 at diagnosis were associated with negative outcomes in progression-free survival and OS. Adjuvant radiotherapy for patients who had LS and for those who cannot undergo grossly total tumor removal resulted in a good outcome.

CONCLUSIONS:

GTR demonstrated better outcomes for solitary PIMM. For recurrent tumors, aggressively repeated surgical resection remained beneficial for selected cases. Adjuvant radiotherapy was a treatment option for LS following operation. We proposed a possible treatment algorithm for solitary PIMM.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Melanoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Melanoma Idioma: En Ano de publicação: 2022 Tipo de documento: Article