Infantile Myofibroma: A Series of 2 Cases with Special Reference to Cytological Features

被引:3
作者
Dey, Soumya [1 ]
Khatun, Farjana [1 ]
Ray, Raktim [1 ]
Barman, Shibsankar [2 ]
Chatterjee, Uttara [1 ]
机构
[1] IPGME&R, Dept Pathol, Kolkata, India
[2] IPGME&R, Dept Pediat Surg, Kolkata, India
关键词
Infantile myofibroma; fibroblastic-myofibroblastic tumors; FNAC; NEEDLE-ASPIRATION-CYTOLOGY; GIANT-CELL FIBROBLASTOMA; DIAGNOSIS; SOLITARY;
D O I
10.1080/15513815.2021.1945173
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Background Infantile myofibromas (IM) are benign soft tissue lesions of childhood and represent a significant portion of the benign spectrum of fibroblastic-myofibroblastic tumors. Cytological diagnosis of these tumors can be challenging because of overlapping morphology and limited case report descriptions. We describe the cytological features and the cytological differential diagnoses. Case report We describe cytological features of two IMs. The main features were the presence of loose clusters and dispersed bland myofibroblasts in varying stages of maturation with traversing blood vessels and myxoid stroma. The cells typically lacked features of atypia, mitoses and significant pleomorphism. Conclusion Diagnosis of IM on the basis of cytology alone can be tricky and definitive diagnosis should be made only after correlating the cytological features with histology. However, bland morphology of differentiating myofibroblasts can aid in cytological diagnosis and help to exclude other malignant spindle cells neoplasms needing preoperative chemotherapy.
引用
收藏
页码:689 / 697
页数:9
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