Systemic mastocytosis with renal light chain amyloidosis: associated non-mast cell disorder or concurrent disease
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Springer Verlag
Abstract
Systemic mastocytosis with an associated hematological neoplasm (SM-AHN) is a rare diagnosis commonly associated with myeloid disorders. Herein, we describe the case of a 53-year-old female diagnosed with systemic mastocytosis (SM) in conjunction with renal light chain amyloidosis (AL) and smoldering myeloma. Although cytokines such as IL-6 may play a role in the proliferation of plasma cells, delays in the diagnosis of SM and paucity of relevant studies cast uncertainty on whether the associated disease is secondary to the mast cells or etiologically independent. To our knowledge, this is the first case of confirmed renal AL disease in conjunction with SM. We review and summarize the available literature describing SM in association with plasma cell disorders. © 2019, Springer-Verlag GmbH Germany, part of Springer Nature.
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Amyloidosis, Plasma cell disorder, Systemic mastocytosis, Immunoglobulin heavy chain, Immunoglobulin kappa chain, Immunoglobulin lambda chain, Interleukin 2 receptor alpha, Lactate dehydrogenase, Stem cell factor receptor, Adult, Al amyloidosis, Albuminuria, Article, Case report, Clinical article, Comorbidity, Disease association, Female, Fluorescence in situ hybridization, Follow up, Gene deletion, Hepatomegaly, Human, Human tissue, Immunofluorescence, Kidney biopsy, Lower limb, Middle aged, Myeloma, Neck tumor, Peripheral edema, Positron emission tomography-computed tomography, Priority journal, Protein electrophoresis, Proteinuria, Pruritus, Skin defect, Splenomegaly, Swelling, Thyroid disease, Thyroid papillary carcinoma, Ultrasound