Bahrami Eshagh, Najafi Masoumeh, Jahanbakhshi Amin, Hatam Jaber, Molanaei Saadat, Ciammella Patrizia, Cozzi Salvatore
Skull Base Research Center, Department of Neurosurgery, Hazrat Rasoul Akram Hospital, Iran University of Medical Sciences, Tehran 1997667665, Iran.
Stem Cell and Regenerative Medicine Research Center, Iran University of Medical Sciences, Tehran 1997667665, Iran.
Brain Sci. 2022 Jul 21;12(7):958. doi: 10.3390/brainsci12070958.
Histiocytic sarcoma (HS) is a rare neoplasm composed of cells with immunohistochemical characteristics of mature histiocytes. It can be disseminated or localized and usually involves the skin, spleen, and gastrointestinal tract. Primary involvement of the vertebral column is extremely rare. We report a 29-year-old female who presented with neck pain and had a destructive 354348 mm lesion in C2 with a paravertebral extension. The initial biopsy did not lead to the correct diagnosis. She later developed dysphagia, and the anterior approach was used for tumor decompression. The diagnosis of cervical histiocytic sarcoma was made, and she underwent radiotherapy. The follow-up MRI showed a marked response to radiotherapy. Here, we report the first case of cervical HS, review all cases of vertebral HS, compare patients' characteristics and clinical courses, and discuss diagnostic nuances and treatment options.
组织细胞肉瘤(HS)是一种罕见的肿瘤,由具有成熟组织细胞免疫组化特征的细胞组成。它可以是播散性的或局限性的,通常累及皮肤、脾脏和胃肠道。脊柱原发性受累极为罕见。我们报告一名29岁女性,她因颈部疼痛就诊,C2椎体有一个35×43×48mm的破坏性病变并向椎旁延伸。最初的活检未能得出正确诊断。她后来出现吞咽困难,采用前路手术进行肿瘤减压。最终诊断为颈椎组织细胞肉瘤,她接受了放疗。随访MRI显示对放疗有明显反应。在此,我们报告首例颈椎HS病例,回顾所有椎体HS病例,比较患者特征和临床病程,并讨论诊断细微差别和治疗选择。