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IgD Multiple Myeloma: a Rare and Aggressive Entity: Report of Three Clinical Cases and Review of the Literature.

2/5 보강
Clinical laboratory 📖 저널 OA 0% 2023: 0/2 OA 2024: 0/2 OA 2025: 0/14 OA 2026: 0/14 OA 2023~2026 2026 Vol.72(3) Multiple Myeloma Research and Treatm
Retraction 확인
출처
PubMed DOI OpenAlex 마지막 보강 2026-04-28

PICO 자동 추출 (휴리스틱, conf 2/4)

유사 논문
P · Population 대상 환자/모집단
환자: a mean age of 38 years
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] Compared to existing literature, our series aligns with the known features of IgD myeloma, including male predominance, lambda light chain involvement, anemia, renal dysfunction, and lytic bone lesions. However, it is distinguished by the unusually young age of the patients, highlighting the need for heightened clinical suspicion in younger individuals presenting with such symptoms.
OpenAlex 토픽 · Multiple Myeloma Research and Treatments Viral-associated cancers and disorders Chronic Myeloid Leukemia Treatments

Chachi EM, Bouabdellah M, Derbal S, Oufir FE, Safir N, Benchekroun L

📝 환자 설명용 한 줄

[BACKGROUND] IgD multiple myeloma is an exceptionally rare subtype, accounting for less than 2% of all multiple myeloma cases.

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↓ .bib ↓ .ris
APA El Mostafa Chachi, Mounya Bouabdellah, et al. (2026). IgD Multiple Myeloma: a Rare and Aggressive Entity: Report of Three Clinical Cases and Review of the Literature.. Clinical laboratory, 72(3). https://doi.org/10.7754/Clin.Lab.2025.250567
MLA El Mostafa Chachi, et al.. "IgD Multiple Myeloma: a Rare and Aggressive Entity: Report of Three Clinical Cases and Review of the Literature.." Clinical laboratory, vol. 72, no. 3, 2026.
PMID 41945733 ↗

Abstract

[BACKGROUND] IgD multiple myeloma is an exceptionally rare subtype, accounting for less than 2% of all multiple myeloma cases.

[METHODS] We report three cases diagnosed at the central biochemistry laboratory of the Ibn Sina University Hospital in Rabat, Morocco, involving young patients with a mean age of 38 years.

[RESULTS] All cases showed a marked male predominance. Clinically, patients presented with frequent bone involvement and renal impairment. Laboratory findings consistently revealed anemia, Bence-Jones proteinuria with a predominance of lambda light chains, hypercalcemia, and variable bone marrow infiltration by plasma cells, reaching up to 88%. The diagnosis is often challenging due to the subtle or absent monoclonal bands on serum protein electrophoresis.

[CONCLUSIONS] Compared to existing literature, our series aligns with the known features of IgD myeloma, including male predominance, lambda light chain involvement, anemia, renal dysfunction, and lytic bone lesions. However, it is distinguished by the unusually young age of the patients, highlighting the need for heightened clinical suspicion in younger individuals presenting with such symptoms.

🏷️ 키워드 / MeSH 📖 같은 키워드 OA만

🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반