Abstract
Avascular necrosis of the femoral head is not specific disease. It occurs as a complication or secondary to various causes. These conditions probably lead to impaired blood supply to the femoral head. The diagnosis of AVNFH is based on clinical findings and supported by specific radiological manifestations. AVNFH occurs as a complication traumatic and non-traumatic disorders. Most cases of AVNFH are non-traumatic and occur secondary to excessive corticosteroid use and alcohol abuse.Other causes include coagulopathies, hemoglobinopathies (sickle cell disease), chronic liver disease ,gout, idiopathic hyperlipidemia, metabolic bone disorders, pregnancy, radiation, chemotherapy, smoking, systemic lupus erythematosus and vasculitis syndromes. Intravascular coagulation appears to be the central event associated with nontraumatic AVNFH , Coagulation may occur secondary to extravascular compression (marrow fat enlargement), vessel wall injury (chemotherapy, radiation), or a thromboembolic event (fat emboli). Magnetic resonance imaging MRI considered the preferred method for diagnosis of occult AVN, since it is more sensitive than bone scan or plain films. Due to the high incidence of bilateral AVN, MRI may pick up AVN in opposite asymptomatic hip. MRI has 90-100% sensitivity for symptomatic disease
AVNFH can be presenting Manifestation for patient with CML as illustrated in table 1
Patient . | Age . | Gender . | site . | Note . | Year . | Reference . |
---|---|---|---|---|---|---|
1 | 24 | Male | Rt Femoral Head | Leukocytecount 96,800/mm3, Platelets count 684,000/mm3, and Hemoglobin 10.4 g/dL. | 2005 | Moon JY, et al. (7) |
2 | 15 | Female | Rt Femoral Head | Leucocyte count of 290 X 109/L,Plateletcount 250 x 109/L, Hemoglobin 10.8 g/dl | 2003 | Gupta D, et al.(8) |
3 | 17 | Male | Rt Femoral Head | Unknown | 1984 | Gibson J, et al.(9) |
4 | 9 | Female | Lt Femoral Head | Leukocytecount 359,000/mm3, Platelets count 809,000/mm3 | 1988 | Salimi Z, et al.(10) |
5 | 17 | Male | Rt Femoral Head | Unknown | 1996 | Leone J, et al.(11) |
6 | 12 | Female | Rt Femoral Head | Unknown | 2013 | Leone J, et al.(12) |
Patient . | Age . | Gender . | site . | Note . | Year . | Reference . |
---|---|---|---|---|---|---|
1 | 24 | Male | Rt Femoral Head | Leukocytecount 96,800/mm3, Platelets count 684,000/mm3, and Hemoglobin 10.4 g/dL. | 2005 | Moon JY, et al. (7) |
2 | 15 | Female | Rt Femoral Head | Leucocyte count of 290 X 109/L,Plateletcount 250 x 109/L, Hemoglobin 10.8 g/dl | 2003 | Gupta D, et al.(8) |
3 | 17 | Male | Rt Femoral Head | Unknown | 1984 | Gibson J, et al.(9) |
4 | 9 | Female | Lt Femoral Head | Leukocytecount 359,000/mm3, Platelets count 809,000/mm3 | 1988 | Salimi Z, et al.(10) |
5 | 17 | Male | Rt Femoral Head | Unknown | 1996 | Leone J, et al.(11) |
6 | 12 | Female | Rt Femoral Head | Unknown | 2013 | Leone J, et al.(12) |
Or can be consequence of therapy with interferon as illustrated in table 2or TKI as illustrated in table 3
Summary of Patients with Chronic Myeloid Leukemia and Associated AVNFH | |||||||
Patient . | Patient (yrs) . | Gender . | Interval from CML dx to development of AVNFH . | Platelet and WBC counts at time of AVNFH dx . | IFNa dose . | Other Rx . | Comment . |
---|---|---|---|---|---|---|---|
1 | 22 | Male | 18 | Platelets, 61-140x109/L; WBC, 2.5-3.5 x 109/L | 5MU/q.o.d. to 2 MU 2x/week | HU pegylated IFN, steroids x 1 week, anegrelide | |
2 | 45 | Female | 54 | Platelets, 120-210 x 109/L; WBC, 15 x 109/L | Varied from 10 MU/day to 5 MU/day | HU, busulfan, ara-C (3 mos) | |
3 | 46 | Female | 6 | Platelets, 160-220 x 109/L; WBC, 8.4-18 x 109/L | 10 MU/day with concurrent ATRA and ara-C | HU | |
4 | 17 | Male | Presenting symptom and symptoms recurred 1 month after starting IFNa and ara-c | Platelets, 895 x 109/L; WBC, 167 x 109/L | Unknown | HU | HU cytoreductiona/w clinical and radiographic improvement of AVNFH |
5 | 25 | Female | 4 yrs | Platelets, 1200 x 109/L;WBC 49 x 109/L | Unknown | HU | ANFH developed when CML entered accelerated phase after 4 yrs of IFNa therapy |
Summary of Patients with Chronic Myeloid Leukemia and Associated AVNFH | |||||||
Patient . | Patient (yrs) . | Gender . | Interval from CML dx to development of AVNFH . | Platelet and WBC counts at time of AVNFH dx . | IFNa dose . | Other Rx . | Comment . |
---|---|---|---|---|---|---|---|
1 | 22 | Male | 18 | Platelets, 61-140x109/L; WBC, 2.5-3.5 x 109/L | 5MU/q.o.d. to 2 MU 2x/week | HU pegylated IFN, steroids x 1 week, anegrelide | |
2 | 45 | Female | 54 | Platelets, 120-210 x 109/L; WBC, 15 x 109/L | Varied from 10 MU/day to 5 MU/day | HU, busulfan, ara-C (3 mos) | |
3 | 46 | Female | 6 | Platelets, 160-220 x 109/L; WBC, 8.4-18 x 109/L | 10 MU/day with concurrent ATRA and ara-C | HU | |
4 | 17 | Male | Presenting symptom and symptoms recurred 1 month after starting IFNa and ara-c | Platelets, 895 x 109/L; WBC, 167 x 109/L | Unknown | HU | HU cytoreductiona/w clinical and radiographic improvement of AVNFH |
5 | 25 | Female | 4 yrs | Platelets, 1200 x 109/L;WBC 49 x 109/L | Unknown | HU | ANFH developed when CML entered accelerated phase after 4 yrs of IFNa therapy |
Summary of Patients with Chronic Myeloid Leukemia and Associated AVNFH | |||||||
Patient . | Patient (yrs) . | Gender . | Interval from CML dx to development of AVN . | Platelet and WBC counts at time of AVN dx . | TKI dose . | Other Rx . | Comment . |
---|---|---|---|---|---|---|---|
1 | 12 | Male | 8 yrs | WBC 5600/mm3 | Start dose 400mg/d; escalated to 600mg/d to achieve complete cytogenetic response | Dx as CML (chronic phase in 2005; started on imatinib 400mg (340mg/m2) after 20 months dose escalated to 600mg/day (continued for 1 yr) Nataraj V et al | |
2 | 34 | female | 3 year | WBC 6000/ mm3 | Failed Imatinib 400mg Then shifted to Dasatinib 100 mg | Developed AVNFH18 months after Dastinib in (CHR, CCR, MMR)yassin et al |
Summary of Patients with Chronic Myeloid Leukemia and Associated AVNFH | |||||||
Patient . | Patient (yrs) . | Gender . | Interval from CML dx to development of AVN . | Platelet and WBC counts at time of AVN dx . | TKI dose . | Other Rx . | Comment . |
---|---|---|---|---|---|---|---|
1 | 12 | Male | 8 yrs | WBC 5600/mm3 | Start dose 400mg/d; escalated to 600mg/d to achieve complete cytogenetic response | Dx as CML (chronic phase in 2005; started on imatinib 400mg (340mg/m2) after 20 months dose escalated to 600mg/day (continued for 1 yr) Nataraj V et al | |
2 | 34 | female | 3 year | WBC 6000/ mm3 | Failed Imatinib 400mg Then shifted to Dasatinib 100 mg | Developed AVNFH18 months after Dastinib in (CHR, CCR, MMR)yassin et al |
Conclusion
From the above mentioned review of literature; 6 patients with CML presented with AVNFH as the initial presentation prior any therapy; five in the era of interferon and two in era with TKIs; one with Imatinib and the other with Dasatinib treatment. Two issues to be considered; either the condition is rare or there is under-reporting of this side effect. Observational studies with proper reporting are required to accurately measure the incidence of this complication which could significantly affect patients' safety and quality of life.
Al-Dewik:Qatar National Research Fund (QNRF): Other: sponsorship.
Author notes
Asterisk with author names denotes non-ASH members.
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