Zombori Tamás, Juhász-Nagy Gréta, Tiszlavicz László, Cserni Gábor, Furák József, Szalontai Klára, Pálföldi Regina
Általános Orvostudományi Kar, Pathologiai Intézet,Szegedi TudományegyetemSzeged, Állomás u. 1., 6725.
Általános Orvostudományi Kar, Sebészeti Klinika,Szegedi TudományegyetemSzeged.
Orv Hetil. 2020 Feb;161(8):313-319. doi: 10.1556/650.2020.31581.
Small-cell lung carcinoma (SCLC) and the rare large-cell neuroendocrine carcinoma belong to the high grade pulmonary neuroendocrine carcinomas. Making the correct diagnosis and selection of treatment modalities require multidisciplinary meetings due to the morphological overlaps, aggressive behaviour and debated therapeutic guidelines of these entities. A 52-year-old woman was admitted to the hospital because of headache, nausea and tenebrous vision. The CT revealed metastatic tumour mass in the occipital lobe and in the cerebellum. Both tumours were removed and resulted in histological diagnosis of metastatic neuroendocrine carcinoma. Chest X-ray established contrast-enhancing lesion in the left lung. Bronchoscopy was performed and histological examination revealed large-cell neuroendocrine carcinoma. Postoperative skull irradiation and small-cell lung cancer chemotherapy protocol were utilized. Due to atelectasis and progression, chest irradiation was initiated, which was interrupted because of novel brain metastases. Further chemotherapy followed the non-small-cell lung cancer protocol. After 3 months, thoracic progression, brain and disseminated bone metastases were diagnosed. After a 14-month-long therapy, the patient deceased. Large-cell neuroendocrine carcinoma has a poor prognosis, the incidence of brain metastasis is 25-50%. In early stage large-cell neuroendocrine carcinoma, lobectomy is the standard treatment and adjuvant chemotherapy should also be considered. Although the non-small-cell lung cancer chemotherapy protocol is approved widely in the treatment of large-cell neuroendocrine carcinoma, the utility of SCLC scheme has also been suggested. Orv Hetil. 2020; 161(8): 313-319.
小细胞肺癌(SCLC)和罕见的大细胞神经内分泌癌属于高级别肺神经内分泌癌。由于这些实体的形态学重叠、侵袭性生物学行为以及存在争议的治疗指南,做出正确诊断和选择治疗方式需要多学科会诊。一名52岁女性因头痛、恶心和视力模糊入院。CT显示枕叶和小脑有转移性肿瘤肿块。切除了这两个肿瘤,组织学诊断为转移性神经内分泌癌。胸部X线检查发现左肺有强化病变。进行了支气管镜检查,组织学检查显示为大细胞神经内分泌癌。采用了术后头颅放疗和小细胞肺癌化疗方案。由于肺不张和病情进展,开始进行胸部放疗,但因出现新的脑转移而中断。随后按照非小细胞肺癌方案进行进一步化疗。3个月后,诊断出胸部进展、脑转移和播散性骨转移。经过14个月的治疗,患者死亡。大细胞神经内分泌癌预后较差,脑转移发生率为25% - 50%。在早期大细胞神经内分泌癌中,肺叶切除术是标准治疗方法,也应考虑辅助化疗。尽管非小细胞肺癌化疗方案在大细胞神经内分泌癌的治疗中得到广泛认可,但也有人建议使用小细胞肺癌方案。《匈牙利医学周报》。2020年;161(8): 313 - 319。