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Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III.
Kahraman, Ayca Burcu; Yaz, Ismail; Gocmen, Rahsan; Aytac, Selin; Metin, Ayse; Kilic, Sara Sebnem; Tezcan, Ilhan; Cagdas, Deniz.
Affiliation
  • Kahraman AB; Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Yaz I; Ihsan Dogramaci Childrens Hospital, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Gocmen R; Department of Pediatric Immunology, Institute of Child Health, Hacettepe University, Ankara, Turkey.
  • Aytac S; Department of Radiology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Metin A; Ihsan Dogramaci Childrens Hospital, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Kilic SS; Department of Pediatrics, Division of Pediatric Hematology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
  • Tezcan I; Department of Pediatrics, Division of Immunology, University of Health Sciences, Ankara City Hospital, Ankara, Turkey.
  • Cagdas D; Department of Pediatrics, Division of Immunology and Rheumatology, Uludag University Faculty of Medicine, Bursa, Turkey.
J Clin Immunol ; 43(6): 1250-1258, 2023 08.
Article in En | MEDLINE | ID: mdl-37014583
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteopetrosis / Leukocyte-Adhesion Deficiency Syndrome Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: J Clin Immunol Year: 2023 Document type: Article Affiliation country: Turkey

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteopetrosis / Leukocyte-Adhesion Deficiency Syndrome Type of study: Diagnostic_studies Limits: Female / Humans / Male Language: En Journal: J Clin Immunol Year: 2023 Document type: Article Affiliation country: Turkey
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