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一项针对77例儿科患者手术切除的头皮和颅骨肿块的研究。

A study of 77 cases of surgically excised scalp and skull masses in pediatric patients.

作者信息

Yoon Soo Han, Park Se-Hyuck

机构信息

Department of Neurosurgery, Ajou University School of Medicine, Suwon, South Korea.

出版信息

Childs Nerv Syst. 2008 Apr;24(4):459-65. doi: 10.1007/s00381-007-0523-2. Epub 2007 Nov 7.

Abstract

OBJECTIVES

Most cases of pediatric scalp and skull masses are either congenital or developmental tumors or diseases, and in many patients, these lesions are accompanied by intracranial extension. Past studies pertaining to these conditions are few, and thus clinical information is as yet inadequate.

MATERIALS AND METHODS

The authors present 75 pediatric patients with 77 cases of surgically treated scalp and skull masses. The most common pathologic condition was Langerhans cell histiocytosis, followed by epidermal cysts, epidermoid and dermoids, scalp hemangiomas, and neurofibromas, in descending order. Intracranial extension was observed in three cases (4%); two cases were malignant tumors that were skull metastasis of a neuroblastoma and a lymphoma, and one case was encephalocele. Lesions followed up because of possible recurrence were 15 cases of Langerhans cell histiocytosis, eight cases of epidermoid and dermoids, two cases of malignant tumors, and one case each of desmoplastic fibroma, myxoma, fibroid dysplasia, and neurofibroma, totaling 29 cases (39%).

CONCLUSION

Although the overall incidence of intracranial extension of pediatric scalp and skull masses is very low and the presence of a malignant tumor or metastatic tumor presenting as a scalp and skull mass is rare, such masses enlarge as time progresses, and there exists a possibility of recurrent disease. Therefore, it is suggested that early surgical resection will afford favorable prognosis for the patients, and meticulous follow-up is necessary in some conditions.

摘要

目的

大多数小儿头皮和颅骨肿块病例为先天性或发育性肿瘤或疾病,且许多患者的这些病变伴有颅内扩展。过去关于这些病症的研究较少,因此临床信息尚不充分。

材料与方法

作者报告了75例小儿患者的77例经手术治疗的头皮和颅骨肿块。最常见的病理情况依次为朗格汉斯细胞组织细胞增多症、表皮样囊肿、表皮样瘤和皮样囊肿、头皮血管瘤及神经纤维瘤。观察到3例(4%)有颅内扩展;2例为恶性肿瘤,分别是神经母细胞瘤和淋巴瘤的颅骨转移,1例为脑膨出。因可能复发而进行随访的病变有15例朗格汉斯细胞组织细胞增多症、8例表皮样瘤和皮样囊肿、2例恶性肿瘤,以及促结缔组织增生性纤维瘤、黏液瘤、纤维发育异常和神经纤维瘤各1例,共29例(39%)。

结论

尽管小儿头皮和颅骨肿块颅内扩展的总体发生率很低,且以头皮和颅骨肿块形式出现的恶性肿瘤或转移性肿瘤很少见,但此类肿块会随时间进展而增大,且存在疾病复发的可能性。因此,建议早期手术切除对患者预后有利,在某些情况下进行细致的随访是必要的。

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