|Year : 2017 | Volume
| Issue : 3 | Page : 278-280
Sudden visual loss as an initial manifestation of chronic myeloid leukemia
Ahmed N Buzaid, Ali M Al-Amri
Department of Internal Medicine, College of Medicine, Imam Abdulrahman Bin Faisal University, King Fahd Hospital of the University, Al-Khobar, Saudi Arabia
|Date of Web Publication||21-Aug-2017|
Ali M Al-Amri
Department of Internal Medicine, King Fahd Hospital of the University, P.O. Box 40182, Al-Khobar 31952
Source of Support: None, Conflict of Interest: None
Chronic myelogenous leukemia (CML) is a pluripotent stem cell disease characterized by anemia, granulocytosis and granulocytic immaturity, basophilia, thrombocytosis and splenomegaly. It is associated with a reciprocal chromosomal translocation t (q34; q11), resulting in a breakpoint cluster region–Abelson fusion gene (Philadelphia chromosome). Ophthalmic manifestations as the first and the only presentation of CML in patients are very rare. Ocular lesions in CML patients are frequently asymptomatic, and thus all patients should undergo an eye evaluation at the initial diagnosis. Here, we report a previously healthy 36-year-old Saudi male who initially presented with progressive loss of vision. On examination, he was found to have a bilateral retinal hemorrhage. The investigations revealed findings consistent with CML. The patient was treated with tyrosine kinase inhibitors, and he had complete remission, including full recovery of his vision.
Keywords: Chronic myelogenous leukemia, retinal hemorrhage, Saudi, visual loss
|How to cite this article:|
Buzaid AN, Al-Amri AM. Sudden visual loss as an initial manifestation of chronic myeloid leukemia. Saudi J Med Med Sci 2017;5:278-80
|How to cite this URL:|
Buzaid AN, Al-Amri AM. Sudden visual loss as an initial manifestation of chronic myeloid leukemia. Saudi J Med Med Sci [serial online] 2017 [cited 2022 Dec 4];5:278-80. Available from: https://www.sjmms.net/text.asp?2017/5/3/278/213304
| Introduction|| |
Among all age groups of Saudis patients with cancer, leukemia is the third most common cancer in males, the fifth in females and fourth in both genders. Chronic myelogenous leukemia (CML) is a rare type of leukemia, accounting for 14% of all leukemias in the United States and 15.3% of all leukemias in Saudi Arabia., CML is a proliferative disorder of the hematopoietic stem cell and it is a genetic disease characterized by the presence of the Philadelphia chromosome, which results from a reciprocal translocation between the chromosomes 9 and 22.,
About 85% of CML patients are diagnosed in the chronic phase, of which 40% are asymptomatic., The breakpoint cluster region–Abelson (BCR–ABL) will disrupt tyrosine kinase activity because of its effect as an oncoprotein, leading to the increased survival of malignant cells. Tyrosine kinase inhibitor (TKI) inhibits the action of BCR–ABL, leading to the death of malignant cells containing the abnormal Philadelphia chromosome.,
| Case Report|| |
The present case reports a 36-year-old Saudi male who presented with loss of vision in the right eye. The patient had no history of cardiac and autoimmune diseases as well as had no family history of blood diseases such as sickle cell anemia, thalassemia or leukemia. The physical examination findings were not suggestive of splenomegaly, lymphadenopathy, cardiac arrhythmias or murmurs.
The patient was referred from the Ophthalmology Clinic at the King Fahd Hospital of the University because the white blood count (WBC) was 543 × 103/L. It was stated that the patient had poor vision in the right eye with central opacity.
The patient had a progressive visual loss in the left eye for 2 weeks before presentation. The visual loss was not associated with pain, fever, redness or any other symptoms. After being seen and examined by a medical team, funduscopic examination showed findings consistent with bilateral retinal hemorrhage and dilatation of blood vessels.
Blood tests were requested, including renal function test, liver function test, blood sugar, calcium and magnesium; all these blood tests were normal as were the coagulation tests. However, complete blood counts revealed profound leukocytosis: WBC count 543 × 103/L. The manual differential count showed 60% polymorph, 11% band, 1% lymph, 1% monocyte, 3% eosinophil, 2% basophil, 9% myelocyte, 3% promyelocyte and 3% blast. Red blood cell count was 4 × 103/L (range: 4.5–6.6), hematocrit was 24% (40–54) and platelet count was 526 × 103/L (140–440). Bone marrow biopsy and peripheral blood film showed hypercellular bone marrow composed of atypical myeloid cells, as shown in [Figure 1]. In addition, chromosomal analysis was positive for the t(9;22) translocation, as shown in [Figure 2]. Fluorescence in situ hybridization identified the BCR–ABL gene fusion. Based on these findings, the patient was diagnosed with CML.
| Discussion|| |
CML is a myeloproliferative disorder that results from expression of the fusion gene BCR–ABL following a chromosomal translocation in the hematopoietic stem cell. The diagnosis of CML is established by increased bone marrow cellularity and identifying a reciprocal translocation between chromosomes 9 and 22 in a hematopoietic stem cell, as shown in [Figure 1] and [Figure 2].
The clinical onset of a disease like CML can be considered as insidious, and some CML patients are diagnosed by chance during their routine checkups. Some presenting symptoms of CML such as angina pectoris, pulmonary insufficiency, priapism and visual loss are not common symptoms. Only 5–10% CML patients present with eye symptoms as the initial presentation at the time of diagnosis.
On clinical examination, splenomegaly is the most common physical finding in a patient with CML. However, in our patient, the spleen was not palpable clinically. In asymptomatic leukemia patients, ocular lesions are often detected, which has led several authors to suggest inclusion of eye examination in the routine evaluation., Our patient had progressive and painless visual loss in the right eye for about 2 weeks before diagnosis. He had an eye examination by the ophthalmologist, and bilateral retinal hemorrhage was diagnosed secondary to CML. The ophthalmic manifestations of CML vary drastically and include intraretinal, subhyaloid and vitreous hemorrhages; nerve fiber layer infarcts; Roth's spots; infiltration of the optic nerve; ischemia and papilledema secondary to raised intracranial pressure.,, In addition to the eye manifestation, it has been reported that CML patients with ophthalmic manifestations have a 5-year lower survival rate than those without these manifestations.
Treatment options for patients with CML are varied and include a potential cure with allogeneic hematopoietic cell transplantation, disease control without a cure using TKIs or palliative therapy with cytotoxic agents.
The treatment of CML depends on the phase of the disease and other factors such as age, response and ability to tolerate therapy, availability of donor and medical comorbidities. The response to TKIs was defined according to clinical, hematological and molecular response, as shown in [Table 1].
|Table 1: Definitions of response to tyrosine kinase inhibitors therapy in chronic myelogenous leukemia|
Click here to view
Assessment of response and follow-up evaluation
The patient was treated with imatinib 400 mg daily. He responded very well to therapy and within 3 months he was not complaining of symptoms. The retinal hemorrhages were healed completely with complete visual recovery. He had a complete hematologic response: complete normalization of peripheral WBC count (<10 × 103/L) and platelet count (<450 × 103/L) sustained for the past 10 years, as shown in [Table 2]. In the first 5 years, BCR–ABL transcript monitor was not available; however, during the last 5 years, the PCR/ABL monitor became available, and subsequently it was measured every 6 months. The last reading of PCR/ABL monitor was 0.00037, as shown in [Table 2].
In summary, this study reports a patient who presented with retinal hemorrhages secondary to CML that lead to blindness as the first manifestation of CML. This case illustrates that CML should be considered as a possible etiology in patients with visual loss. Therefore, ophthalmic evaluation is needed in these patients for early identification and treatment to restore visual function.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Cancer Incidence Report Saudi Arabia 2010. Council of Health Services; 2014.
Kasper DL. Harrison's Principles of Internal Medicine. 16th
ed. United States: McGraw-Hill Professional Book Group; 2005.
Granatowicz A, Piatek CI, Moschiano E, El-Hemaidi I, Armitage JD, Akhtari M. An overview and update of chronic myeloid leukemia for primary care physicians. Korean J Fam Med 2015;36:197-202.
Huang PK, Sanjay S. Visual disturbance as the first symptom of chronic myeloid leukemia. Middle East Afr J Ophthalmol 2011;18:336-8. [Full text]
Saglio G, Kim DW, Issaragrisil S, le Coutre P, Etienne G, Lobo C, et al.
Nilotinib versus imatinib for newly diagnosed chronic myeloid leukemia. N Engl J Med 2010;362:2251-9.
Rennie I. Ophthalmic manifestations of childhood leukaemia. Br J Ophthalmol 1992;76:641.
Reddy SC, Jackson N, Menon BS. Ocular involvement in leukemia – A study of 288 cases. Ophthalmologica 2003;217:441-5.
Sharma T, Grewal J, Gupta S, Murray PI. Ophthalmic manifestations of acute leukaemias: The ophthalmologist's role. Eye (Lond) 2004;18:663-72.
Jabbour E, Kantarjian HM, Saglio G, Steegmann JL, Shah NP, Boqué C, et al.
Early response with dasatinib or imatinib in chronic myeloid leukemia: 3-year follow-up from a randomized phase 3 trial (DASISION). Blood 2014;123:494-500.
[Figure 1], [Figure 2]
[Table 1], [Table 2]