Mathew S, Rappaport K, Ali S Z, Busseniers A E, Rosenthal D L
John K. Frost Cytopathology Laboratory, Department of Pathology, Johns Hopkins Hospital, Baltimore, Maryland 21287, USA.
Acta Cytol. 1997 Jul-Aug;41(4):955-60. doi: 10.1159/000332767.
To define and elaborate the cytomorphologic features of primary and metastatic ameloblastoma (ABL) on fine needle aspiration (FNA) and to discuss the differential diagnosis with closely related entities and review the cytologic literature on the subject.
A retrospective study consisting of five cases of ameloblastomas, primary in the mandible (n = 3) and metastases (n = 2), diagnosed by FNA cytology with appropriate cytohistologic correlation, was done. Smears were stained with the Diff-Quik and Papanicolaou methods. Hematoxylin and eosin-stained sections of paraffin block as well as sections from the surgically resected specimens were also reviewed.
The smears were hypercellular and occasionally showed tissue fragments of basaloid cells with peripheral palisading. A distinct, two-cell population was seen, consisting of small, hyperchromatic, basaloid-type cells and scattered larger cells with more open chromatin. Occasional fragments of mesenchymal cells with more elongated nuclei and ample, clear cytoplasm were also noted. Malignant cases that metastasized showed prominent cytologic pleomorphism, cellular crowding with molding and a high mitotic/karyorrhectic index.
In the right clinical setting and with proper radiologic evidence, the cytologic features of primary and metastatic ameloblastoma are unique. Diagnostic problems may arise when these lesions are pleomorphic and frankly malignant, especially at metastatic sites, such as the lung. FNA, therefore, is a valuable diagnostic tool in the initial diagnosis and follow-up of patients with a history of ameloblastoma.
明确并阐述原发性和转移性成釉细胞瘤在细针穿刺抽吸(FNA)中的细胞形态学特征,讨论其与密切相关疾病的鉴别诊断,并回顾关于该主题的细胞学文献。
进行了一项回顾性研究,包括5例经FNA细胞学诊断并结合适当细胞组织学相关性的成釉细胞瘤病例,其中3例为下颌骨原发性,2例为转移性。涂片采用Diff-Quik和巴氏染色法染色。还复查了石蜡块苏木精和伊红染色切片以及手术切除标本的切片。
涂片细胞丰富,偶尔可见基底样细胞组织碎片,周边呈栅栏状排列。可见明显的双细胞群,由小的、核深染的基底样细胞和散在的较大细胞组成,后者染色质更疏松。还注意到偶尔有间充质细胞碎片,核更长,胞质丰富、清亮。发生转移的恶性病例显示出明显的细胞多形性、细胞拥挤伴细胞巢形成以及高有丝分裂/核溶解指数。
在合适的临床背景下并具备适当的影像学证据时,原发性和转移性成釉细胞瘤的细胞学特征是独特的。当这些病变具有多形性且明显为恶性时,尤其是在转移部位如肺部,可能会出现诊断问题。因此,FNA是成釉细胞瘤病史患者初始诊断和随访中的一种有价值的诊断工具。