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Naslov:Unmasking indolent systemic mastocytosis in patients with unexplained or treatment-refractory osteoporosis : a case series with diagnostic and therapeutic implications
Avtorji:ID Jankovski, Lucia (Avtor)
ID Herman, Rok (Avtor)
ID Rakuša, Matej (Avtor)
ID Kopač, Peter (Avtor)
ID Kačar, Mark (Avtor)
ID Škerget, Matevž (Avtor)
ID Janež, Andrej (Avtor)
ID Jensterle Sever, Mojca (Avtor)
Datoteke:URL URL - Izvorni URL, za dostop obiščite https://www.mdpi.com/2218-273X/16/6/821
 
Jezik:Angleški jezik
Tipologija:1.01 - Izvirni znanstveni članek
Organizacija:Logo UKC LJ - Univerzitetni klinični center Ljubljana
Povzetek:Indolent systemic mastocytosis (ISM) is an under-recognised cause of secondary osteoporosis, and skeletal fragility may be the only presenting feature, delaying diagnosis. We describe four adults referred to a tertiary endocrinology service for unexplained osteoporosis or low-trauma fractures, in whom systemic mastocytosis (SM) was identified during work-up. All had elevated basal serum tryptase (41.4–87.0 µg/L), bone-marrow biopsy showing atypical mast cells and the KIT D816V variant; cutaneous lesions were absent in every case. Three patients fulfilled WHO 2022 criteria for ISM. The fourth had coexistent JAK2 V617F-positive post-essential-thrombocythaemia myelofibrosis and was classified as SM with associated haematological neoplasm (SM-AHN); his mast cell clone (tryptase 43.7 µg/L; KIT D816V VAF 0.391%) behaved indolently and contributed clinically through osteoporosis alone, illustrating that an indolent mast cell component can be overlooked when a chronic myeloid neoplasm dominates the picture. Presentations ranged from an isolated low-energy L5 fracture in a 55-year-old man, to multiple vertebral compression fractures despite denosumab in a 71-year-old woman with primary hyperparathyroidism, to severe wasp-sting anaphylaxis in a 43-year-old man. After multidisciplinary review, all received intravenous zoledronic acid with vitamin D repletion; KIT-targeted therapy is under consideration in selected patients. Although causal inferences cannot be drawn from four retrospectively identified cases, the series illustrates how ISM may be missed in unexplained or treatment-refractory osteoporosis—particularly in younger men, those with prior severe anaphylaxis, and those fracturing on antiresorptive therapy—and supports combining basal serum tryptase with high-sensitivity peripheral-blood KIT D816V testing, in line with the WHO/ICC/AIM-ECNM 2022–2024 criteria. Prospective studies are needed.
Ključne besede:indolent systemic mastocytosis, osteoporosis, bone mineral density
Status publikacije:Objavljeno
Verzija publikacije:Objavljena publikacija
Leto izida:2026
Št. strani:str. 1-15
Številčenje:Vol. 16, iss. 6, [article no.] 821
PID:20.500.12556/DiRROS-30394 Novo okno
UDK:616.4
ISSN pri članku:2218-273X
DOI:10.3390/biom16060821 Novo okno
COBISS.SI-ID:280057859 Novo okno
Opomba:Nasl. z nasl. zaslona; Opis vira z dne 27. 5. 2026;
Datum objave v DiRROS:24.06.2026
Število ogledov:35
Število prenosov:17
Metapodatki:XML DC-XML DC-RDF
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Gradivo je del revije

Naslov:Biomolecules
Skrajšan naslov:Biomolecules
Založnik:MDPI AG
ISSN:2218-273X
COBISS.SI-ID:519952921 Novo okno

Gradivo je financirano iz projekta

Financer:ARIS - Javna agencija za znanstvenoraziskovalno in inovacijsko dejavnost Republike Slovenije
Številka projekta:P3-0298-2019
Naslov:Geni, hormonske in osebnostne spremembe pri metabolnih motnjah

Licence

Licenca:CC BY 4.0, Creative Commons Priznanje avtorstva 4.0 Mednarodna
Povezava:http://creativecommons.org/licenses/by/4.0/deed.sl
Opis:To je standardna licenca Creative Commons, ki daje uporabnikom največ možnosti za nadaljnjo uporabo dela, pri čemer morajo navesti avtorja.

Sekundarni jezik

Jezik:Slovenski jezik
Ključne besede:indolentna sistemska mastocitoza, agregacija proteinov, osteoporoza, mineralna gostota kosti


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