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原发性颈囊状水瘤:一例罕见病例报告。

Primary cervical hydatid cyst: A rare case report.

作者信息

Rahimi Mohammad Tareq, Hares Roohullah, Rahman Haseeb, Shinwari Mohammad Amin, Khaliqi Soghra, Hares Sheila

机构信息

Department of Paediatric Surgery, French Medical Institute for Mothers and Children, Kabul, Afghanistan.

Department of Paediatric Surgery, French Medical Institute for Mothers and Children, Kabul, Afghanistan.

出版信息

Int J Surg Case Rep. 2023 Jun;107:108349. doi: 10.1016/j.ijscr.2023.108349. Epub 2023 May 24.

Abstract

INTRODUCTION AND IMPORTANCE

Hydatid cyst is a zoonotic parasitic disease caused by Echinococcus granulosis. Occurrence in the head and neck is quite uncommon even in endemic areas. The diagnosis of an isolated cystic neck mass is still a challenge due to the presence of similar congenital cystic lesions and benign tumors in the neck. Imaging is useful, but sometimes they cannot identify a definitive diagnosis. The treatment of choice is exclusively surgical excision, combined with chemotherapy. Histopathology confirms the definitive diagnosis.

CASE PRESENTATION

We present a case of an 8-year-old boy with no history of surgery or trauma, who complained of an isolated left posterior neck mass since one year. All radiological items lead to suspect a cystic lymphangioma. Excisional biopsy under general anesthesia was done. The cystic mass was totally resected and the diagnosis was further confirmed by histopathology.

CLINICAL DISCUSSION

Cervical hydatid cyst is mostly a misdiagnosed condition, majority of hydatid cyst cases are asymptomatic and vary on the basis of their locations. The differential diagnosis includes cystic lymphangioma, branchial cleft cyst, bronchogenic, thoracic duct, esophageal duplication cysts, pseudocysts and benign tumors.

CONCLUSION

Isolated cervical hydatid cyst is rarely reported yet, it must be considered in any cases of cystic cervical mass, particularly in endemic areas. Imaging modalities are sensitive in diagnosing cystic lesions, yet sometimes they cannot identify the exact etiology of the lesion. Furthermore, Prevention of hydatid disease is more favorable than surgical excision.

摘要

引言与重要性

包虫囊肿是一种由细粒棘球绦虫引起的人畜共患寄生虫病。即使在流行地区,头颈部出现该病也相当罕见。由于颈部存在类似的先天性囊性病变和良性肿瘤,孤立性颈部囊性肿块的诊断仍然具有挑战性。影像学检查很有用,但有时无法明确诊断。治疗的首选方法是单纯手术切除,并结合化疗。组织病理学可确诊。

病例介绍

我们报告一例8岁男孩,无手术或外伤史,自一年前起主诉左后颈部有一孤立肿块。所有影像学检查结果均怀疑为囊性淋巴管瘤。在全身麻醉下进行了切除活检。囊性肿块被完全切除,组织病理学进一步证实了诊断。

临床讨论

颈部包虫囊肿大多被误诊,大多数包虫囊肿病例无症状,且根据其位置不同而有所差异。鉴别诊断包括囊性淋巴管瘤、鳃裂囊肿、支气管源性囊肿、胸导管囊肿、食管重复囊肿、假性囊肿和良性肿瘤。

结论

孤立性颈部包虫囊肿的报道仍然很少,在任何颈部囊性肿块病例中都必须考虑到,特别是在流行地区。影像学检查对囊性病变的诊断很敏感,但有时无法确定病变的确切病因。此外,预防包虫病比手术切除更可取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a6e2/10238829/fe6869bcdb99/gr1.jpg

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