Info
🌱來自: castleman_disease
Classification
- CD: Castleman disease;
- POEMS: Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal plasma cell disorder, Skin changes
- TAFRO: Thrombocytopenia, Ascites(or Anasarca), reticulin Fibrosis(or Fever), Renal dysfunction, and Organomegaly
- NOS: not otherwise specified
FDC: Follicular dendritic cell
Siblings
- A 41-Year-Old Man with Dyspnea, Fever, and Lymphadenopathy
- CT of the Chest, Abdomen, and Pelvis
- Histopathological Presentation
- Bone marrow examination
- Diagnosis
- Definition
- Epidemiology
- Pathogenesis
- Pahtogenesis (continued)
- Histopathological of Castleman Disease
- Histopathological of Castleman Disease (continued)
- Follicles With Mantle Zones With An “Onion Skin” Pattern
- Hyaline vascular Castleman disease
- Grading of pathologic features seen in iMCD
- Algorithmic approach for assessment of lymph node with features of CD
- Diagnostic criteria for iMCD
- Significant clinical, histologic, and immunologic overlap
- Conditions Characterized by Inflammation and Differential Diagnosis for iMCD
- Diagnostic criteria for iMCD-TAFRO
- Severity scoring of iMCD
- The management of UCD
- Management of iMCD
- IL-6 pathway
- IL-6 Inhibitors
- Siltuximab for multicentric Castleman’s disease
- Definitions of Treatment Response
- Which type of biopsy would you use in order to prevent the delay of a Castleman disease diagnosis?
- According to guidelines, which type of therapy is most optimal for your patient with idiopathic multicentric Castleman disease?
- What is required for the diagnosis of iMCD?
- Which of the following is true regarding the diagnosis of iMCD?
- Take home message
- [[thank_you_for_
your_time_and_attention.md|Thank you for
your time and attention]] - Table of Contents