[组织细胞坏死性淋巴结炎成人和儿童患者的临床特征和治疗]。

Q3 Medicine 北京大学学报(医学版) Pub Date : 2024-06-18
Xiuwen Fei, Si Liu, Bo Wang, Aimei Dong
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All the 81 patients underwent lymph node biopsy, and 77.8%(63/81) of the patients showed that most of the structures in the lymph nodes were destroyed or disappeared, and 16.0%(13/81) of the lymph nodes were still in existence, hyperplasia and normal lymph node were 1.2%(1/81) respectively, and 3.7%(3/81) had normal lymph node structures. Immunohistochemical staining was performed in 67 cases. The percentages of CD3<sup>+</sup> and CD68(KP1)<sup>+</sup> were respectively 97.0%(65/67), and MPO<sup>+</sup> were 94.0%(63/67). In the study, 51 patients (63.0%, 51/81) were treated with glucocorticoid therapy after diagnosis. The median time for temperature to return to normal was 1.0(1.0, 4.0) days after glucocorticoid therapy. when the glucocorticoid treatment worked best, the body temperature could drop to normal on the same day. There were significant differences in length of stay, predisposing factors, chills, the rate of increase in high-sensitivity CRP, antibiotic and glucocorticoid treatment between the adults and children groups (<i>P</i> < 0.05).</p><p><strong>Conclusion: </strong>In clinical practice, if there are cases with unexplained fever, superficial lymph node enlargement, and reduced white blood cells as clinical characteristics, and general antibiotics treatment is ineffective, histiocytic necrotic lymphadenitis should be considered. Lymph node biopsy should be performed as early as possible to clarify the diagnosis, reduce misdiagnosis and mistreatment, and symptomatic treatment should be the main treatment. 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引用次数: 0

摘要

目的分析组织细胞坏死性淋巴结炎(HNL)的临床资料,比较儿童与成人的异同,加深临床医生对该病的认识,提高诊断率,减少误诊误治:收集北京大学第一医院2010年1月至2023年8月经活检确诊的组织细胞坏死性淋巴结炎住院患者的临床资料,分析组织细胞坏死性淋巴结炎的临床特征、实验室检查、病理特征、抗生素和糖皮质激素治疗情况及预后。根据年龄分组,比较儿童组(<16 岁)与成人组(≥16 岁)在临床特征、实验室检查、治疗和预后方面的差异:81 名入选患者中,男性 42 人,女性 39 人。年龄中位数为 21(14,29)岁,病程中位数为 20.0(13.0,30.0)天,住院时间中位数为 13.0(10.0,15.0)天。首发症状为发热、淋巴结肿大和两者兼有。所有患者都有不同部位和大小的淋巴结肿大,96.3%(81 例中有 78 例)的患者有颈淋巴结病,50.6%(81 例中有 41 例)的患者有双侧颈淋巴结病,55.6%(81 例中有 45 例)的患者有锁骨上、腋窝或腹股沟淋巴结病,淋巴结直径中位数为 20.0(20.0,30.0)毫米。只有一名患者没有发烧,其他 80 名患者均有发烧,最高体温中位数为 39.0(38.0,39.8)℃。伴随症状:皮疹(8.6%,7/81)、乏力(34.6%,28/81)、盗汗(8.6%,7/81)、寒战(25.3%,25/81)、肌肉酸痛(13.6%,11/81)和关节痛(6.2%,5/81)。肝脾肿大 17 例(21.0%,17/81),其中脾肿大 12 例(70.6%,12/17)。68.8%(55/80)的患者白细胞(WBC)计数下降,47.5%(38/80)的患者淋巴细胞(LY)比例升高,53.4%(39/73)的患者高敏 C 反应蛋白(CRP)升高,79.2%(57/72)的患者红细胞沉降率(ESR)升高,22.2%(18/81)的患者丙氨酸转氨酶(ALT)升高,27.2%(22/81)的患者天门冬氨酸转氨酶(AST)升高,81.6%(62/76)的患者乳酸脱氢酶(LDH)升高。所有 81 例患者均接受了淋巴结活检,结果显示 77.8%(63/81)的患者淋巴结结构大部分被破坏或消失,16.0%(13/81)的淋巴结仍然存在,增生和正常淋巴结分别为 1.2%(1/81),3.7%(3/81)的淋巴结结构正常。对 67 个病例进行了免疫组化染色。CD3+和CD68(KP1)+的比例分别为97.0%(65/67),MPO+的比例为94.0%(63/67)。研究中,51 名患者(63.0%,51/81)在确诊后接受了糖皮质激素治疗。糖皮质激素治疗后体温恢复正常的中位时间为1.0(1.0,4.0)天。当糖皮质激素治疗效果最佳时,体温可在当天降至正常。成人组和儿童组在住院时间、诱发因素、寒战、高敏CRP升高率、抗生素和糖皮质激素治疗等方面存在明显差异(P<0.05):在临床实践中,如果病例出现不明原因的发热、浅表淋巴结肿大、白细胞减少等临床特征,且一般抗生素治疗无效,则应考虑组织细胞坏死性淋巴结炎。应尽早进行淋巴结活检以明确诊断,减少误诊误治,并以对症治疗为主。糖皮质激素治疗有确切疗效。
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[Clinical characteristics and treatment in adults and children with histiocytic necroti-zing lymphadenitis].

Objective: To analyze the clinical data of histiocytic necrotizing lymphadenitis(HNL), comparing the similarities and differences between children and adults, to deepen the understanding of the disease by clinical physicians, and to improve diagnostic rate and reduce misdiagnosis and mistreatment.

Methods: The clinical data of hospitalized patients with histiocytic necrotizing lymphadenitis diagnosed by biopsy from January 2010 to August 2023 in Peking University First Hospital were collec-ted, and the clinical features, laboratory examinations, pathological features, treatments with antibiotics and glucocorticoids, and prognosis of histiocytic necrotic lymphadenitis were analyzed. Grouped based on age, the differences of clinical characteristics, laboratory tests, treatment, and prognosis between the children group (< 16 years old) and the adult group (≥16 years old) were compared.

Results: Among the 81 enrolled patients, there were 42 males and 39 females. The median age was 21(14, 29) years, the median duration of disease was 20.0(13.0, 30.0) days, and the median length of hospital stay was 13.0 (10.0, 15.0) days. The first symptoms were fever, lymphadenopathy, and both. All the patients had enlarged lymph nodes with different parts and sizes, 96.3% (78 of 81) of the patients had cervical lymphadenopathy, 50.6% (41 of 81) had bilateral cervical lymphadenopathy, 55.6% (45 of 81) had supraclavicular, axillary or inguinal lymphadenopathy, and the median lymph node diameter was 20.0(20.0, 30.0) mm. Only one patient had no fever, the other 80 patients had fever, the median peak body temperature was 39.0(38.0, 39.8) ℃. Accompanying symptoms: rash (8.6%, 7/81), fatigue (34.6%, 28/81), night sweating (8.6%, 7/81), chills (25.3%, 25/81), muscle soreness (13.6%, 11/81), and joint pain (6.2%, 5/81). There were 17 cases (21.0%, 17/81) of hepatosplenomegaly, of which 12 cases (70.6%, 12/17) were splenomegaly. 68.8%(55/80) of patients had a decrease in white blood cell (WBC) count, with 47.5%(38/80)increased in lymphocyte(LY)proportion, 53.4%(39/73) increased in high-sensitivity C-reactive protein(CRP), 79.2%(57/72) increased in erythrocyte sedimentation rate(ESR), 22.2%(18/81) increased in alanine transaminase(ALT), 27.2%(22/81) elevated in aspartate transaminase(AST), and 81.6%(62/76) elevated in lactate dehydrogenase(LDH). All the 81 patients underwent lymph node biopsy, and 77.8%(63/81) of the patients showed that most of the structures in the lymph nodes were destroyed or disappeared, and 16.0%(13/81) of the lymph nodes were still in existence, hyperplasia and normal lymph node were 1.2%(1/81) respectively, and 3.7%(3/81) had normal lymph node structures. Immunohistochemical staining was performed in 67 cases. The percentages of CD3+ and CD68(KP1)+ were respectively 97.0%(65/67), and MPO+ were 94.0%(63/67). In the study, 51 patients (63.0%, 51/81) were treated with glucocorticoid therapy after diagnosis. The median time for temperature to return to normal was 1.0(1.0, 4.0) days after glucocorticoid therapy. when the glucocorticoid treatment worked best, the body temperature could drop to normal on the same day. There were significant differences in length of stay, predisposing factors, chills, the rate of increase in high-sensitivity CRP, antibiotic and glucocorticoid treatment between the adults and children groups (P < 0.05).

Conclusion: In clinical practice, if there are cases with unexplained fever, superficial lymph node enlargement, and reduced white blood cells as clinical characteristics, and general antibiotics treatment is ineffective, histiocytic necrotic lymphadenitis should be considered. Lymph node biopsy should be performed as early as possible to clarify the diagnosis, reduce misdiagnosis and mistreatment, and symptomatic treatment should be the main treatment. Glucocorticoids therapy has a definite therapeutic effect.

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北京大学学报(医学版)
北京大学学报(医学版) Medicine-Medicine (all)
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9815
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