Overview
Angiofollicular lymph node hyperplasia is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Lymph node hyperplasia
Very frequent (80-99%)HP:0002716
Constitutional symptom
Frequent (30-79%)HP:0025142
Elevated C-reactive protein level
Frequent (30-79%)HP:0011227
Elevated sedimentation rate
Frequent (30-79%)HP:0003565
Follicular hyperplasia
Frequent (30-79%)HP:0002729
Gastro pain
Frequent (30-79%)HP:0002027
Increased circulating interleukin 6 concentration
Frequent (30-79%)HP:0030783
Low number of red blood cells or hemoglobin
Frequent (30-79%)HP:0001903
Swollen lymph nodes in centre of chest
Frequent (30-79%)HP:0100721
Tiredness
Frequent (30-79%)HP:0012378
Weight loss
Frequent (30-79%)HP:0001824
Abdominal mass
Occasional (5-29%)HP:0031500
Belly bloating
Occasional (5-29%)HP:0003270
Coughing
Occasional (5-29%)HP:0012735
Decreased MCV
Occasional (5-29%)HP:0025066
Digestive system disease
Occasional (5-29%)HP:0011024
Generalized lymphadenopathy
Occasional (5-29%)HP:0008940
Kidney pain
Occasional (5-29%)HP:0030157
Nausea and vomiting
Occasional (5-29%)HP:0002017
Yellowing of the skin
Occasional (5-29%)HP:0000952
Anasarca
Very rare (1-4%)HP:0012050
Blood in urine
Very rare (1-4%)HP:0000790
Bowel obstruction
Very rare (1-4%)HP:0005214
Difficulty breathing
Very rare (1-4%)HP:0002094
Myelofibrosis
Very rare (1-4%)HP:0011974
Renal insufficiency
Very rare (1-4%)HP:0000083
Restrictive cardiomyopathy
Very rare (1-4%)HP:0001723
Thrombocytopenia
Very rare (1-4%)HP:0001873
Ureteral obstruction
Very rare (1-4%)HP:0006000
Related Conditions
Angiofollicular lymph node hyperplasia, hyaline-vascular type(child)
Angiofollicular lymph node hyperplasia, plasma cell type(child)
Castleman's superficial pseudotumour, involving skin(child)
Castleman disease co-occurrent with infection caused by Human herpesvirus 8(child)
Angiolymphoid hyperplasia with eosinophilia(child)
Multicentric Castleman disease(child)
Localized Castleman disease(child)
Castleman's disease with IgM -associated neuropathy(child)
Enlargement of lymph nodes(parent)
Hyperplastic lymph node(parent)
Atypical lymphoproliferative disorder(parent)
Immunoproliferative disorder(parent)
Quick Facts
- SNOMED CT
- 207036003
- UMLS CUI
- C0017531
- Fully Specified Name
- Castleman's disease (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 29
- Known Treatments
- 1
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.