Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Ihsan Dogramaci Childrens Hospital, Hacettepe University Faculty of Medicine, Ankara, Turkey.
J Clin Immunol. 2023 Aug;43(6):1250-1258. doi: 10.1007/s10875-023-01479-7. Epub 2023 Apr 4.
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.
To discuss the distinguishing clinical, radiological, and laboratory features of LAD-III.
This study included the clinical, radiological, and laboratory characteristics of twelve LAD-III patients.
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).
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.
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。
讨论 LAD-III 的独特临床、放射学和实验室特征。
本研究纳入了 12 例 LAD-III 患者的临床、放射学和实验室特征。
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)。
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。