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白细胞黏附缺陷症 III 型患者的临床和类骨硬化影像学表现。

Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III.

机构信息

Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.

Ihsan Dogramaci Childrens Hospital, Hacettepe University Faculty of Medicine, Ankara, Turkey.

出版信息

J Clin Immunol. 2023 Aug;43(6):1250-1258. doi: 10.1007/s10875-023-01479-7. Epub 2023 Apr 4.

Abstract

BACKGROUND

Leukocyte and platelet integrin function defects are present in leukocyte adhesion deficiency type III (LAD-III) due to mutations in FERMT3. Additionally, osteoclast/osteoblast dysfunction develops in LAD-III.

AIM

To discuss the distinguishing clinical, radiological, and laboratory features of LAD-III.

METHODS

This study included the clinical, radiological, and laboratory characteristics of twelve LAD-III patients.

RESULTS

The male/female ratio was 8/4. The parental consanguinity ratio was 100%. Half of the patients had a family history of patients with similar findings. The median age at presentation and diagnosis was 18 (1-60) days and 6 (1-20) months, respectively. The median leukocyte count on admission was 43,150 (30,900-75,700)/μL. The absolute eosinophil count was tested in 8/12 patients, and eosinophilia was found in 6/8 (75%). All patients had a history of sepsis. Other severe infections were pneumonia (66.6%), omphalitis (25%), osteomyelitis (16.6%), gingivitis/periodontitis (16%), chorioretinitis (8.3%), otitis media (8.3%), diarrhea (8.3%), and palpebral conjunctiva infection (8.3%). Four patients (33.3%) received hematopoietic stem cell transplantation (HSCT) from HLA-matched-related donors, and one deceased after HSCT. At initial presentation, 4 (33.3%) patients were diagnosed with other hematologic disorders, three patients (P5, P7, and P8) with juvenile myelomonocytic leukemia (JMML), and one (P2) with myelodysplastic syndrome (MDS).

CONCLUSION

In LAD-III, leukocytosis, eosinophilia, and bone marrow findings may mimic pathologies such as JMML and MDS. In addition to non-purulent infection susceptibility, patients with LAD-III exhibit Glanzmann-type bleeding disorder. In LAD-III, absent integrin activation due to kindlin-3 deficiency disrupts osteoclast actin cytoskeleton organization. This results in defective bone resorption and osteopetrosis-like radiological changes. These are distinctive features compared to other LAD types.

摘要

背景

由于 FERMT3 基因突变,白细胞黏附缺陷 III 型(LAD-III)患者存在白细胞和血小板整合素功能缺陷。此外,LAD-III 还会出现破骨细胞/成骨细胞功能障碍。

目的

讨论 LAD-III 的独特临床、放射学和实验室特征。

方法

本研究纳入了 12 例 LAD-III 患者的临床、放射学和实验室特征。

结果

男女比例为 8:4。父母近亲结婚比例为 100%。一半的患者有类似表现的家族史。就诊时和确诊时的中位年龄分别为 18(1-60)天和 6(1-20)个月。入院时白细胞计数的中位数为 43150(30900-75700)/μL。在 12 例患者中检测了绝对嗜酸性粒细胞计数,发现嗜酸性粒细胞增多的有 6/8(75%)例。所有患者均有脓毒症病史。其他严重感染包括肺炎(66.6%)、脐炎(25%)、骨髓炎(16.6%)、牙龈炎/牙周炎(16%)、脉络膜炎(8.3%)、中耳炎(8.3%)、腹泻(8.3%)和睑结膜感染(8.3%)。4 例(33.3%)患者接受了 HLA 匹配相关供体的造血干细胞移植(HSCT),其中 1 例在 HSCT 后死亡。在初次就诊时,4 例(33.3%)患者被诊断为其他血液系统疾病,3 例(P5、P7 和 P8)为幼年型粒单核细胞白血病(JMML),1 例(P2)为骨髓增生异常综合征(MDS)。

结论

在 LAD-III 中,白细胞增多、嗜酸性粒细胞增多和骨髓发现可能类似于 JMML 和 MDS 等病理情况。除了非化脓性感染易感性外,LAD-III 患者还表现出 Glanzmann 型出血性疾病。在 LAD-III 中,由于 kindlin-3 缺乏导致整合素激活缺失,破坏了破骨细胞的肌动蛋白细胞骨架组织。这导致了骨吸收缺陷和类骨质硬化的影像学改变。与其他 LAD 类型相比,这些是独特的特征。

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