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婴儿纤维性错构瘤的细胞学诊断:一例罕见软组织病变的病例报告

Cytologic diagnosis of fibrous hamartoma of infancy: a case report of a rare soft tissue lesion.

作者信息

Gupta Ruchika, Singh Sompal

机构信息

Department of Pathology, Maulana Azad Medical College and Hindu Rao Hospital, New Delhi, India.

出版信息

Acta Cytol. 2008 Mar-Apr;52(2):201-3. doi: 10.1159/000325480.

Abstract

BACKGROUND

Fibrous hamartoma of infancy (FHI) is a rare, benign lesion seen in the first 2 years of life. Despite adequate histopathologic descriptions, reports of it in the cytology literature are rare.

CASE

A 6-month-old male infant presented with an asymptomatic nodule in left anterior axillary fold. The nodule was noticed 6 weeks before presentation. On local examination, it was mobile and rubbery. Considering the endemicity, a presumptive clinical diagnosis of tuberculous lymphadenitis was made. Fine needle aspiration yielded moderately cellular smears composed of short spindle cells in a greasy background admixed with a few adipocytes. No mitosis or abnormal chromatin pattern was seen. In view of the young age of the patient, a cytologic impression of benign lesion or hamartoma was made. Excision of the nodule and histopathologic examination revealed it as FHI.

CONCLUSION

The cytologist should be aware of the cytologic features of FHI, so that in the proper clinical setting this diagnosis can be made with certainty. The mixture of adipose tissue and bland spindle cells is helpful to differentiate this lesion from other infantile soft tissue lesions.

摘要

背景

婴儿纤维性错构瘤(FHI)是一种罕见的良性病变,见于出生后2年内。尽管有充分的组织病理学描述,但细胞学文献中关于它的报道却很少。

病例

一名6个月大的男婴,左前腋窝皱襞处出现一个无症状结节。该结节在就诊前6周被发现。局部检查时,它可活动且质地似橡胶。考虑到地方流行情况,临床初步诊断为结核性淋巴结炎。细针穿刺抽吸得到中等细胞涂片,涂片由油腻背景中的短梭形细胞组成,并混有一些脂肪细胞。未见有丝分裂或异常染色质模式。鉴于患者年龄较小,做出良性病变或错构瘤的细胞学诊断。结节切除及组织病理学检查显示为婴儿纤维性错构瘤。

结论

细胞学家应了解婴儿纤维性错构瘤的细胞学特征,以便在适当的临床情况下能够准确做出该诊断。脂肪组织和平淡的梭形细胞混合有助于将此病变与其他婴儿软组织病变区分开来。

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