Results 31 to 40 of about 403,362 (211)

Cutaneous lymphoplasmacytic lymphoma

open access: yesJournal of the American Academy of Dermatology, 1998
We report a case of cutaneous lymphoplasmacytic lymphoma with multiple recurrences. The patient's disease has been controlled with local radiotherapy, excision, and low dose chemotherapy. During the 9 years of his disease, he has not experienced extracutaneous involvement.
J I, Allbritton, T D, Horn
openaire   +2 more sources

Primary Bone Lymphoplasmacytic Lymphoma Presenting with Spinal Cord Compression: A Case Report

open access: yesTurkish Journal of Hematology, 2013
Primary bone lymphoma is a rare disease, and the main pathological type is diffuse large B-cell lymphoma. The occurrence of follicular, marginal zone and lymphoplasmacytic lymphomas is rare.
Yang Lei   +4 more
doaj   +1 more source

Uncommon IgG Lymphoplasmacytic Lymphoma: Case report

open access: yesPakistan Journal of Medical Research, 2022
Lymphoplasmacytic lymphoma is quite rare neoplasm of mature B lymphocytes. It accounts for less than 1% of Non Hodgkin Lymphoma in west. Its incidence is 10 times less in Asian countries.In majority of cases, patients have a circulating monoclonal IgM ...
Syeda Mah Ali, Naila Raza
doaj   +2 more sources

Diffuse Involvement of Primary Colorectal Lymphoma Simulating Ulcerative Colitis [PDF]

open access: yesJournal of Pathology and Translational Medicine, 2019
Diffuse involvement of colorectal lymphoma masquerading as colitis is a very rare presentation of primary colorectal lymphoma. Detecting occult lymphoma is difficult in the setting of diffuse colonic involvement with no definite mass and inflammatory ...
Ji-Ye Kim   +3 more
doaj   +1 more source

Upper airway obstruction caused by primary lymphoplasmacytic lymphoma of the retropharyngeal space: a case report

open access: yesThe Egyptian Journal of Otolaryngology, 2021
Background Primary malignant tumours of the retropharyngeal space are rare with only a few case reports in the literature. Lymphoplasmacytic lymphoma is a rare subtype of non-Hodgkin lymphoma and is very rarely found as a primary tumour of the ...
Chinyere N. Asoegwu   +2 more
doaj   +1 more source

Disseminated strongyloidiasis complicated by alveolar hemorrhage, meningitis, and septic shock treated with albendazole and subcutaneous ivermectin

open access: yesInternational Journal of Infectious Diseases, 2019
The case of a patient with disseminated strongyloidiasis following chemotherapy for lymphoplasmacytic lymphoma is presented.
A. Balkhair   +6 more
doaj   +1 more source

Pleural fluid MYD88 L265P mutation supporting diagnosis and decision to treat extramedullary Waldenstrom’s macroglobulinemia: a case report

open access: yesJournal of Medical Case Reports, 2020
Background Our case of a patient with untreated lymphoplasmacytic lymphoma/Waldenstrom’s macroglobulinemia with extramedullary pleural effusion is the first documented case of pleural fluid MYD88 L265P mutation status in a community hospital setting. Our
Martin Barnes   +4 more
doaj   +1 more source

Primary CNS lymphoplasmacytic lymphoma: A case report and review of literature

open access: yesHematology/Oncology and Stem Cell Therapy, 2013
Lymphoplasmacytic lymphoma is a chronic lymphoproliferative disorder characterized by a proliferation of plasma cells, small lymphocytes, plasmacytoid lymphocytes and the production of monoclonal IgM.
Kamal KS Abbi   +5 more
doaj   +1 more source

Short term results of vaccination with adjuvanted recombinant varicella zoster glycoprotein E during initial BTK inhibitor therapy for CLL or lymphoplasmacytic lymphoma

open access: yesLeukemia, 2020
Reactivation of latent infection by varicella zoster (VZR) usually causes shingles with less common complications including postherpetic neuralgia, retinitis, cranial nerve palsies, myelitis, meningitis, cerebrovascular events, pancreatitis, hepatitis ...
C. Zent   +11 more
semanticscholar   +1 more source

Mu heavy chain disease with MYD88 L265P mutation: an unusual manifestation of lymphoplasmacytic lymphoma

open access: yesDiagnostic Pathology, 2022
Background Mu heavy chain disease is a rare lymphoid neoplasm characterized by vacuolated bone marrow plasma cells and secretion of defective mu immunoglobulin heavy chains. The biological basis of mu heavy chain disease is poorly understood.
Vandana Baloda   +9 more
doaj   +1 more source

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