Results 31 to 40 of about 1,092 (158)

Biclonal Gammopathy in Chronic Lymphocytic Leukemia: Case Report and Review of the Literature

Oman Medical Journal, 2015
Monoclonal gammopathies are frequently seen in B-cell malignancies. Monoclonal proteins are seen in a significant proportion of patients with chronic lymphocytic leukemia (CLL), which is a clonal disorder of mature B cells.
Nafila Al-Riyami, Khalil Al-Farsi, Khalfan Al-Amrani, Sameera Al-Harrasi, Mohammed Al-Huneini, Salam Al-Kindi   +5 more
doaj   +1 more source

Acute Lymphoblastic Leukemia Presenting With Severe Acute Kidney Injury Requiring Hemodialysis due to Kidney Infiltration: A Case Report

Clinical Case Reports, Volume 14, Issue 7, July 2026.
ABSTRACT A 66‐year‐old man presented with dialysis‐dependent acute kidney injury without cytopenia or peripheral blasts. Kidney biopsy revealed leukemic infiltration and led to the diagnosis of Philadelphia chromosome‐negative B‐acute lymphoblastic leukemia.
Semin Cho, Soyean Kwon, Jeong Hwan Park, Jin Hyun Park, Ki Hwan Kim, Jin Soo Kim, Eun Youn Roh, In Sil Choi, Ji Eun Kim, Song Yi Park   +9 more
wiley   +1 more source

A 32‐Year‐Old Man With an Cardiomyopathy

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Scleredema is a sclerosing dermatosis of unknown etiology, characterized by non‐punctate, weakly infiltrated skin thickening and swelling, which can lead to the development of cardiomyopathy. Scleredema‐associated cardiomyopathy is at present poorly understood.
Yuting Zou, Shan Li, Tong Chen, Yi Li
wiley   +1 more source

Chronic Inflammatory Demyelinating Polyneuropathy (CIDP): A Comprehensive Review of Types, Pathophysiology, and Treatment Approaches

Brain and Behavior, Volume 16, Issue 5, May 2026.
Chronic inflammatory demyelinating polyneuropathy is an autoimmune disorder causing demyelination, leading to distal weakness, sensory loss, and autonomic dysfunction. Immune activation triggers macrophage‐mediated myelin damage and conduction failure.
Ayesha Khan, Arsal Khan, Kuldeep Dalpat Rai, Anzel Saeed, Harsh Kumar, Aneesh Kumar Sangtiani, Tehreem Fatima, Muhammad Tanveer Alam, Faiza Rajput, Sakshi Chawla, Hussain Haider Shah, Humaira Kalam   +11 more
wiley   +1 more source

Macroglobulinemia de Waldenströn: comunicación de un caso

Anales de la Facultad de Medicina, 2008
La macroglobulinemia de Waldenström (MW) es una rara neoplasia hematológica, caracterizada por la proliferación linfoplasmocitaria, con producción monoclonal de inmunoglobulina M (IgM) e infiltración medular.
Franco Romaní, José Cuadra, Fernando Atencia, Carlos Canelo   +3 more
doaj  

Low Dose Pegylated Interferon Alpha as a First‐Line Treatment for Necrobiotic Xanthogranuloma

JEADV Clinical Practice, Volume 5, Issue 1, Page 215-218, March 2026.
ABSTRACT Necrobiotic xanthogranuloma (NXG) is a rare, progressive granulomatous disorder frequently associated with monoclonal gammopathy, particularly monoclonal gammopathy of undetermined significance (MGUS). It typically presents with indurated to ulcerative yellowish plaques or nodules, often with ocular involvement.
Ishana Dixit, Charmaine Vanessa S. Chamberlin, Pablo Fernandez‐Peñas   +2 more
wiley   +1 more source

Neurological Peculiarities of POEMS Syndrome: Experience From a Brazilian University Center

Muscle &Nerve, Volume 73, Issue 3, Page 421-426, March 2026.
ABSTRACT Aim Polyneuropathy, organomegaly, endocrinopathy, monoclonal protein, and skin changes (POEMS) syndrome is a rare paraneoplastic syndrome associated with significant neurologic morbidity. Better understanding of the manifestations of this disease is crucial to early diagnosis and improvement of prognosis.
Renan Fabri Rosenstein, Jose Pedro Soares Baima, Thales Dalessandro Meneguin Pereira, Gracia Aparecida Martinez, Carlos Otto Heise, Angelina Maria Martins Lino   +5 more
wiley   +1 more source

CIDP With and Without Monoclonal Gammopathy of Undetermined Significance (MGUS): Comparison of Clinical Phenotype, Diagnostic Features, and Treatment Response

Journal of the Peripheral Nervous System, Volume 31, Issue 1, March 2026.
ABSTRACT Background and Aims Monoclonal gammopathy of undetermined significance (MGUS) occurs in some patients with chronic inflammatory demyelinating polyneuropathy (CIDP), but its impact on clinical phenotype and treatment response remains unclear.
R. van Veen, A. E. Baars, I. N. van Doorn, M. Michael, S. R. M. Bus, M. C. Broers, W. L. van der Pol, P. A. Van Doorn, J. Drenthen, C. Verhamme, J. M. I. Vos, I. N. van Schaik, H. S. Goedee, L. Wieske, B. C. Jacobs, F. Eftimov, for the ICOS Consortium   +16 more
wiley   +1 more source

Compresión del plexo lumbosacro por plasmocitoma: mieloma múltiple de cadenas ligeras tipo lambda

Revista Médica Herediana, 2015
Se presenta el caso de una mujer de 51 años que desarrolló paraparesia y una masa abdominal palpable más pérdida de peso en el lapso de cuatro meses. La masa destruía la 5ª vértebra lumbar y se extendía a los tejidos blandos adyacentes. En suero se halló
Oscar G. Pamo, Robert Cumpa, César Chian   +2 more
doaj  

Osteomalacia Following Iron Infusion Therapy in a Patient With Rendu‐Osler‐Weber Syndrome: F‐18‐FDG PET/CT Discrimination of a Stress Fracture in the Setting of a Musculoskeletal Tumor Mimic

Clinical Case Reports, Volume 14, Issue 2, February 2026.
ABSTRACT This case report highlights a rare occurrence of osteomalacia induced by hypophosphatemia secondary to ferric carboxymaltose (FCM) therapy in a patient with hereditary hemorrhagic telangiectasia (HHT, or Rendu‐Osler‐Weber syndrome). A 21‐year‐old man presented with left tibial pain without prior trauma, accompanied by severe hypophosphatemia ...
Ioannis S. Vasios, Pipitsa N. Valsamaki, Konstantinos Tilkeridis, Savvas Deftereos, Efthymios Iliopoulos   +4 more
wiley   +1 more source