Chan A C L, Chan J K C
Department of Pathology, Queen Elizabeth Hospital, Hong Kong.
Histopathology. 2002 Nov;41(5):392-403. doi: 10.1046/j.1365-2559.2002.01461.x.
Pulmonary sclerosing haemangioma is a rare benign tumour with a characteristic variegated histological pattern. In this retrospective study we aimed to identify features that can aid in making a correct diagnosis and avoiding potential pitfalls at the time of intra-operative frozen section.
Twenty cases of pulmonary sclerosing haemangioma with intra-operative frozen section were reviewed. The four major histological patterns (solid, sclerotic, papillary and haemorrhagic) were found in various combinations in the frozen sections. In 17 cases, three or more patterns were present. There could be focal areas mimicking epithelioid haemangioendothelioma or carcinoid tumour. Intra-operative imprint/scrape cytology served as a helpful adjunct in confirming the cytological blandness, although occasional atypical cells could be present. An intra-operative frozen section diagnosis of 'sclerosing haemangioma' or 'benign tumour' was given in 14 cases; the diagnosis was deferred in six cases. Retrospective analysis of the deferred cases showed that a definitive intra-operative diagnosis could have been made in three, because three or more major histological patterns were present. One case showed a pure papillary pattern at frozen section, mimicking the appearance of papillary adenocarcinoma (primary or secondary), bronchioloalveolar carcinoma, epithelioid mesothelioma or papillary adenoma; two tumours from a patient with multicentric disease showed widespread significant cytological atypia in the tumours raising a serious consideration of malignancy.
A diagnosis of pulmonary sclerosing haemangioma can be made at intra-operative frozen sections in most cases based on the tumour circumscription and variegated histological patterns. When only a single histological pattern is identified or when there is significant cytological atypia, distinction from other tumours can be problematic, and the diagnosis is best deferred.
肺硬化性血管瘤是一种罕见的良性肿瘤,具有特征性的斑驳组织学模式。在这项回顾性研究中,我们旨在确定有助于做出正确诊断并避免术中冰冻切片时潜在陷阱的特征。
回顾了20例术中进行冰冻切片的肺硬化性血管瘤病例。在冰冻切片中发现了四种主要组织学模式(实性、硬化性、乳头状和出血性)的各种组合。17例中存在三种或更多模式。可能存在模仿上皮样血管内皮瘤或类癌肿瘤的局灶性区域。术中印片/刮片细胞学检查有助于确认细胞的温和性,尽管偶尔可能会出现非典型细胞。14例术中冰冻切片诊断为“硬化性血管瘤”或“良性肿瘤”;6例诊断延迟。对延迟病例的回顾性分析表明,其中3例本可以做出明确的术中诊断,因为存在三种或更多主要组织学模式。1例在冰冻切片时显示为纯乳头状模式,类似于乳头状腺癌(原发性或继发性)、细支气管肺泡癌、上皮样间皮瘤或乳头状腺瘤的表现;1例多中心疾病患者的两个肿瘤在肿瘤中显示出广泛的明显细胞学异型性,严重怀疑为恶性肿瘤。
大多数情况下,基于肿瘤的边界和斑驳的组织学模式,术中冰冻切片可诊断肺硬化性血管瘤。当仅识别出单一组织学模式或存在明显的细胞学异型性时,与其他肿瘤的鉴别可能存在问题,最好延迟诊断。