Pancytopenia: Difference between revisions
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**[[Immunosuppressive therapy|Immunosuppressants]], [[chemotherapy]], [[Radiation therapy|radiation]] |
**[[Immunosuppressive therapy|Immunosuppressants]], [[chemotherapy]], [[Radiation therapy|radiation]] |
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**Antiseizure: [[carbamazepine]], [[levetiracetam]], [[phenytoin]], [[phenobarbital]], [[valproate]] |
**Antiseizure: [[carbamazepine]], [[levetiracetam]], [[phenytoin]], [[phenobarbital]], [[valproate]] |
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**Gout: [[Allergic bronchopulmonary aspergillosis]], [[colchicine]] |
**Gout: [[Allopurinol|Allergic bronchopulmonary aspergillosis]], [[colchicine]] |
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**Antibiotics: coadministration of [[TMP-SMX]] and [[methotrexate]], [[albendazole]], [[chloramphenicol]], [[cidofovir]], [[dapsone]], [[foscarnet]], [[ganciclovir]], [[linezolid]], [[quinine]], [[Sulfonamide|sulfonamides]], [[zidovudine]] |
**Antibiotics: coadministration of [[TMP-SMX]] and [[methotrexate]], [[albendazole]], [[chloramphenicol]], [[cidofovir]], [[dapsone]], [[foscarnet]], [[ganciclovir]], [[linezolid]], [[quinine]], [[Sulfonamide|sulfonamides]], [[zidovudine]] |
||
**NSAIDs: [[aspirin]], [[diclofenac]], [[ibuprofen]], [[indomethacin]], [[phenylbutazone]], [[Salicylate|salicylates]], [[sulindac]] |
**NSAIDs: [[aspirin]], [[diclofenac]], [[ibuprofen]], [[indomethacin]], [[phenylbutazone]], [[Salicylate|salicylates]], [[sulindac]] |
Latest revision as of 16:14, 28 August 2023
Background
- Combination of anemia (<120-130), neutropenia (<1.8), and platelet (<150)
Clinical Manifestations
- Increased infections, from leukopenia
- Bleeding, from thrombocytopenia
- Angina and other hypoxemic symptoms, from anemia
Differential Diagnosis
- See also aplastic anemia
- Congenital causes (chronic pancytopenia)
- Telomere diseases: dyskeratosis congenita (early hair graying, pulmonary fibrosis, cirrhosis)
- Fanconi anemia (short statue, café-au-lait spots, skeletal abnormalities, urogenital abnormalities)
- GATA2 deficiency (persistent or unusual infections)
- CTLA4 deficiency (intestinal disease, adenopathy, infections, autoimmune disorders)
- Schwachman-Diamond syndrome (skeletal abnormalities, exocrine pancreatic dysfunction)
- Wiskott-Aldrich syndrome (eczema, recurrent infections, low IgM, elevated IgA/E)
- Medication-induced
- Immunosuppressants, chemotherapy, radiation
- Antiseizure: carbamazepine, levetiracetam, phenytoin, phenobarbital, valproate
- Gout: Allergic bronchopulmonary aspergillosis, colchicine
- Antibiotics: coadministration of TMP-SMX and methotrexate, albendazole, chloramphenicol, cidofovir, dapsone, foscarnet, ganciclovir, linezolid, quinine, sulfonamides, zidovudine
- NSAIDs: aspirin, diclofenac, ibuprofen, indomethacin, phenylbutazone, salicylates, sulindac
- Anti-thyroid: methimazole, propylthiouracil
- Cardiovascular: aspirin, amiodarone, captopril, lisinopril, nifedipine, quinidine, ticlopidine
- Diuretics: acetazolamide, furosemide, thiazides
- GI: cimetidine, nizatidine
- Psychiatric: bupropion, lithium, valproate
- Exposures: benzene, MDMA, glue, pesticides, radiation, organic solvents
- Decreased production
- Infection
- Viral
- Epstein-Barr virus: chronic active EBV and primary infection that results in hemophagocytic lymphohistiocytosis
- Parvovirus B19: usually transient, but can also cause pure red cell aplasia
- Cytomegalovirus, if immunocompromised
- Hepatitis A virus
- Human immunodeficiency virus
- Dengue virus
- Bacterial
- Mycobacterium tuberculosis, in the context of disseminated disease
- Leptospira
- Brucella
- Bartonella henselae and Bartonella quintana, causing bacillary angiomatosis involving liver and spleen
- Mycoplasma pneumoniae, associated with fulminant infection and the presence of cold agglutinin disease
- Ehrlichia chaffeensis, causing hemophagocytic lymphohistiocytosis
- Fungal
- Pneumocystis jirovecii, from bone marrow necrosis
- Parasitic
- Viral
- Malignancy
- Other
- Nutritional
- Vitamin B12 deficiency
- May be from underlying severe caloric restriction, eating disorder, bariatric surgery, malabsorption, or alcohol use
- Infection
- Increased destruction with decreased production: autoimmune disorders, PNH, hematologic malignancies, HLH, sepsis
- Increased destruction (hemolysis with increased reticulocytes): Evan syndrome, thrombotic microangiopathy, DIC
- Sequestration (splenomegaly): portal hypertension, cirrhosis, infections, autoimmune disorders, myeloproliferative neoplasm, leukemia, lymphoma, storage diseases
Investigations
- Initial investigations:
- Review prior CBCs to determine chronicity
- CBC with differential and reticulocyte count
- Peripheral blood film
- Lytes/creatinine, uric acid, LDH
- Liver panel
- Coags
- Iron studies
- ESR/CRP
- Consider the following, based on initial workup:
- Then consider the following, based on initial workup:
- Flow cytometry
- Tuberculosis or fungal workup
- US/CT/MRI/PET-CT
- Bone marrow aspirate and biopsy