Jobst S B, Ljung B M, Gilkey F N, Rosenthal D L
Acta Cytol. 1983 May-Jun;27(3):299-305.
We present the first case report of an olfactory neuroblastoma (esthesioneuroblastoma) diagnosed by cytologic examination. The patient was a 40-year-old male who had a 13-year history of "adenocarcinoma" of the nasal cavity until the correct diagnosis of olfactory neuroblastoma was made cytologically from pleural fluid shortly before his death. The cells had the typical features of rosette formation, scanty elongated cytoplasm, clustering of cells and nuclear compression resulting in an "onion-skin" appearance. Surgical specimens, several biopsies and fine needle aspiration of a metastatic deposit in a lymph node all showed, retrospectively, features of esthesioneuroblastoma. Electron microscopy showed membrane-bound dense-core secretory granules. Autopsy findings revealed multiple metastases but no tumor at the original site; that tumor had been treated with high-dose radiation therapy as well as systemic chemotherapy. Olfactory neuroblastoma is a rare tumor, but it is important to recognize because it has a better prognosis than the more commonly encountered malignancies of the nose.
我们报告首例通过细胞学检查确诊的嗅神经母细胞瘤(感觉神经母细胞瘤)病例。患者为一名40岁男性,鼻腔“腺癌”病史长达13年,直至其临终前不久从胸腔积液中通过细胞学检查正确诊断为嗅神经母细胞瘤。细胞具有典型的菊形团形成、细长细胞质稀少、细胞聚集以及核受压导致“洋葱皮”样外观的特征。回顾性分析,手术标本、多次活检以及淋巴结转移灶的细针穿刺抽吸物均显示出嗅神经母细胞瘤的特征。电子显微镜检查显示有膜结合的致密核心分泌颗粒。尸检结果显示存在多处转移,但原发部位无肿瘤;该肿瘤曾接受高剂量放射治疗以及全身化疗。嗅神经母细胞瘤是一种罕见肿瘤,但因其预后比鼻腔更常见的恶性肿瘤更好,所以识别它很重要。