Pancytopenia
Simultaneous leukopenia, nonregenerative anemia, and thrombocytopenia; not a disease itself - rather, a group of laboratory findings that can result from multiple causes.
By Tilley, Larry P. ; Smith, Francis W.K. ; Sleeper, Meg M. ; Brainard, Benjamin M. in Blackwell's Five-Minute Veterinary Consult: Canine and Feline
Overview
Pancytopenia requires a thorough diagnostic evaluation, including bone marrow examination and blood tests, to identify the underlying cause, which can include infections like FeLV, FIV, parvovirus, and anaplasmosis. Treatment involves addressing the specific clinical situation, including supportive measures such as aggressive antibiotic therapy and blood transfusions. Medication should be carefully chosen based on the clinical context, and it is essential to avoid drugs that may suppress blood cell production or trigger immune-mediated destruction. Follow-up care includes daily examinations, temperature monitoring, and periodic complete blood counts to monitor the patient's progress. The prognosis for pancytopenia depends on the underlying cause and may often be guarded.
Symptoms
Lethargy, Petechial hemorrhage, Repeated febrile episodes
Causes
FeLV, FIV, parvovirus, anaplasmosis
Diagnosis
Bone marrow examination, blood tests, underlying conditions
See the full listTreatments
Antibiotic therapy and blood transfusions
See the full listMedication
Should be appropriate for the clinical situation; see specific causes.
See the full listFollow-up
Daily examination, monitoring of body temp, periodic CBC
See the full list
Basics
- Pathophysiology
- Mechanisms may include decreased production of cells in the bone marrow or increased peripheral use, destruction, or sequestration; one or more of these mechanisms may occur together.
- Decreased production occurs when pluripotent, multipotent, or committed stem cells are destroyed, their proliferation or differentiation is suppressed, or the maturation of differentiated cells is delayed or arrested.
- If pluripotent stem cells are affected, pancytopenia develops; if committed stem cells are involved, cytopenia of the specific cell type develops.
- Increased use and destruction of cells typically results in increased production in the bone marrow. At least 2–3 days are required before increased production begins to have an effect on peripheral blood cell counts, and peak output usually takes about a week; thus, the rate of use or destruction necessary to cause cytopenia is not as great during the first few days of disease as it is later.
- Sequestration of cells in the microcirculation, especially that of the spleen, intestine, and lungs, can cause cytopenia of the cell type involved.
- Systems Affected
Hemic/lymphatic/immune—bone marrow, spleen, lymph nodes, and other lymphocytic tissues; depending on the cause, these organs can be affected by cellular depletion, degeneration, necrosis, hyperplasia, dysplasia, or dyscrasia; changes may occur alone or in combination.
- Incidence/Prevalence
Pancytopenia is an uncommon occurrence and does not always occur with the causes listed (see Causes). The incidence is reported as 2.4% in dogs and 2.8% in cats.
- Geographic Distribution
Unless the cause of pancytopenia is an infectious agent that is localized to a certain region (e.g., leishmaniasis, histoplasmosis), no specific geographic distribution exists.
- Signalment
- Dogs and cats.
- No age, sex, or breed predilection.
- Risk Factors
Vary with individual cause

Diagnosis
Signs
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Causes
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Tests
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Lorem ipsum dolor sit amet, consectetur adipiscing elit. Idem iste, inquam, de voluptate quid sentit? Sed tamen intellego quid velit. Est enim effectrix multarum et magnarum voluptatum. An potest cupiditas finiri? Quis istud possit, inquit, negare? Nunc haec primum fortasse audientis servire debemus. Multoque hoc melius nos veriusque quam Stoici.
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Idem iste, inquam, de voluptate quid sentit? Sed tamen intellego quid velit. Est enim effectrix multarum et magnarum voluptatum. An potest cupiditas finiri? Quis istud possit, inquit, negare? Nunc haec primum fortasse audientis servire debemus. Multoque hoc melius nos veriusque quam Stoici.
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Idem iste, inquam, de voluptate quid sentit? Sed tamen intellego quid velit. Est enim effectrix multarum et magnarum voluptatum. An potest cupiditas finiri? Quis istud possit, inquit, negare? Nunc haec primum fortasse audientis servire debemus. Multoque hoc melius nos veriusque quam Stoici.
Lorem ipsum dolor sit amet, consectetur adipiscing elit. Idem iste, inquam, de voluptate quid sentit? Sed tamen intellego quid velit. Est enim effectrix multarum et magnarum voluptatum. An potest cupiditas finiri? Quis istud possit, inquit, negare? Nunc haec primum fortasse audientis servire debemus. Multoque hoc melius nos veriusque quam Stoici.

Treatment
Supportive treatment depends on the clinical situation and includes aggressive antibiotic therapy and blood component transfusions.
Treatment of the underlying condition is paramount.
Medication
Drug(s) of choice
Treatment should be appropriate for the clinical situation (i.e., the degree to which each cell population is decreased, presence of fever or infection, and established or suspected specific diagnoses); see specific causes.
Contradictions
Drugs that may suppress hematopoiesis or trigger immune‐mediated destruction (see Causes). Nonsteroidal anti‐inflammatory drugs, clopidogrel, or other drugs that may interfere with platelet function if thrombocytopenia present.
Precautions
Because of the patient’s potentially compromised immune status, glucocorticoids and other immunosuppressive drugs should be used only when necessary (e.g., when an immune component is suspected) and with extreme care and frequent monitoring.
Alternative drug(s)
Recombinant Hematopoietic Growth Factors: Recombinant human granulocyte colony‐stimulating factor (rhG‐CSF) 1–5 μg/kg/day SC; stimulates neutrophil production, may result in development of antibodies against endogenous G‐CSF. Recombinant human erythropoietin (rhEPO)—initial dosage 100 U/kg SC, 3 times/week; stimulates erythropoiesis, may result in development of antibodies against endogenous EPO, darbepoetin may also be considered.
Follow-up
Patient monitoring
- Daily physical examination, including frequent monitoring of body temperature.
- Periodic CBC—frequency depends on severity of cytopenia, age, general physical condition of the patient, and underlying cause.
Prevention/Avoidance
- Castration of cryptorchid males (to prevent development of a Sertoli or interstitial cell tumor).
- Vaccination for infectious diseases.
- Frequent monitoring of CBC in cancer patients receiving chemotherapy or radiation therapy.
Possible complications
- Hemorrhage.
- Sepsis.
Expected course and prognosis
- Depends on the underlying cause.
- Often a guarded prognosis is warranted.
Zoonotic potential
- Tularemia, if this is the underlying cause.
- An owner can contract histoplasmosis from the same source as the patient.
Pregnancy/fertility/breastfeeding
Stress of underlying disease may cause abortion; see respective topics for the effects of different causes on pregnancy.
Suggested Reading
- Brazzell JL, Weiss DJ. A retrospective study of aplastic pancytopenia in the dog: 9 cases (1996–2003). Vet Clin Pathol 2006, 35:413–417.
- Weiss DJ. Aplastic anemia. In: Weiss DJ, Wardrop KJ, eds., Schalm’s Veterinary Hematology, 6th ed. Ames, IA: Blackwell, 2010, pp. 256–260.
- Weiss, DJ. New insights into the physiology and treatment of acquired myelodysplastic syndromes and aplastic pancytopenia. Vet Clin North Am Small Anim Pract 2003, 33(6):1317–1334.
- Weiss DJ, Evanson OA. A retrospective study of feline pancytopenia. Comp Haematol Int 2000, 1:50–55.
- Weiss DJ, Evanson OA, Sykes J. A retrospective study of canine pancytopenia. Vet Clin Pathol 1999, 28:83–88.