Hypereosinophilic Syndrome (HES) is a rare disorder causing persistently high eosinophil levels, leading to organ damage and inflammation.
White Blood Cells
Leukemoid Reaction
Leukemoid reaction is a benign, reactive process with elevated LAP & no Philadelphia chromosome, unlike malignant CML.
Causes of Atypical Lymphocytes (Reactive Lymphocytes)
Atypical lymphocytes are activated immune cells, often seen in infections. Their unique look aids diagnosis, but distinguishing it from cancer is important.
Chediak-Higashi Syndrome
Chediak-Higashi syndrome (CHS) is a rare genetic disorder characterized by oculocutaneous albinism, immune deficiency, and neurological decline.
Diffuse Large B-Cell Lymphoma (DLBCL)
Learn about Diffuse Large B-Cell Lymphoma (DLBCL) and its diagnosis, treatment with R-CHOP, and management of relapsed disease.
Chediak-Higashi Syndrome
Chediak-Higashi syndrome (CHS) is a rare genetic disorder characterized by oculocutaneous albinism, immune deficiency, and neurological decline.
Chronic Myeloid Leukemia Treatment Strategies
Chronic Myeloid Leukemia Treatment: TKIs are the main therapy, targeting the BCR::ABL1 gene. Chemotherapy & stem cell transplant are also used.
Neutrophilia (High Neutrophils) & Absolute Neutrophilia
Discover causes & implications of high neutrophils, from general neutrophilia to absolute neutrophilia, a key blood cell elevation.
Eosinophilic Esophagitis (EoE)
EoE: Chronic esophageal inflammation. Dysphagia, food impaction. Diagnosis: endoscopy, biopsies. Treatment: diet, meds, dilation.
AL Amyloidosis (Primary Amyloidosis)
AL amyloidosis occurs when misfolded light-chain proteins deposit in organs. Prompt treatment improves outcomes.
Sjögren’s Syndrome
Sjögren’s syndrome: An autoimmune disease causing dry eyes, mouth. Systemic effects is possible. Early diagnosis & management are key.
Waldenström Macroglobulinemia
Waldenström Macroglobulinemia (WM): Rare lymphoma, excess IgM. Causes fatigue, neuropathy, & hyperviscosity. Early diagnosis & tailored treatment are key.