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一名未接受肾移植的23岁木村病男性患者:叙利亚的罕见病例报告。

A 23-year-old male patient with Kimura's disease without renal transplantation: a rare case report from Syria.

作者信息

Alsmoudi Hasan, Sleiay Mouhammed, Almohamed Ahmad, Hamsho Suaad, Alhadla Ahmad, Alqreea Mohammed, Alakhras Abdulkareem

机构信息

Faculty of Medicine, Hama University.

Syrian Medical Scientific Researchers Team (SMSR Team), Hama.

出版信息

Ann Med Surg (Lond). 2024 Jul 1;86(8):4927-4931. doi: 10.1097/MS9.0000000000002341. eCollection 2024 Aug.

Abstract

INTRODUCTION AND IMPORTANCE

Kimura's disease (KD) is a chronic, nonmalignant inflammatory disorder that primarily affects subcutaneous tissue. It is typically characterized by painless nodules in the head and neck regions, accompanied by elevated eosinophil and serum IgE levels. The purpose of this case study is to elucidate this rare disease, particularly in the Asian region and Syria, and to explore diagnostic and therapeutic methodologies with the objective of mitigating the number of undiagnosed patients suffering from this disease.

CASE PRESENTATION

A 23-year-old male patient presented to the Ear, Nose, and Throat (ENT) Department of the hospital with symptoms that had been initiated 7 months prior. The primary symptoms were pain and swelling in the left preauricular area, followed by subsequent swelling in the right preauricular area the next day. The patient experienced severe, intermittent pain, generalized pruritus, and systemic manifestations, including fever, chills, fatigue, malaise, anorexia, and a weight loss of 20 kg over the course of seven months. A fine-needle aspiration of the left parotid gland revealed the presence of lymphocytes at various maturation stages, with no evidence of abnormal cells. A diagnosis of KD was subsequently confirmed.

CLINICAL DISCUSSION

To our knowledge, this case represents the second documented instance of KD in Syria. Furthermore, our case is among the extremely rare instances of KD in a patient without a history of renal transplantation.

CONCLUSION

Further research is essential to ascertain the actual prevalence of this condition and to identify the most effective management strategies.

摘要

引言与重要性

木村病(KD)是一种主要累及皮下组织的慢性非恶性炎症性疾病。其典型特征为头颈部无痛性结节,伴有嗜酸性粒细胞增多和血清IgE水平升高。本病例研究的目的是阐明这种罕见疾病,特别是在亚洲地区和叙利亚的情况,并探索诊断和治疗方法,以减少未被诊断出患有该疾病的患者数量。

病例介绍

一名23岁男性患者因7个月前出现的症状就诊于医院耳鼻喉科。主要症状为左耳前区疼痛和肿胀,次日右耳前区也出现肿胀。患者经历了严重的间歇性疼痛、全身瘙痒以及全身症状,包括发热、寒战、疲劳、不适、厌食,在7个月内体重减轻了20千克。对左侧腮腺进行细针穿刺活检显示存在处于不同成熟阶段的淋巴细胞,未发现异常细胞。随后确诊为木村病。

临床讨论

据我们所知,该病例是叙利亚有记录的第二例木村病病例。此外,我们的病例是极为罕见的无肾移植病史的木村病患者。

结论

进一步的研究对于确定这种疾病的实际患病率以及确定最有效的管理策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4ce/11305731/dd52f0219006/ms9-86-4927-g001.jpg

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