Myeloid Sarcoma in an Eyelid That Developed during Chemotherapy for Acute Myeloid Leukemia

Introduction

Myeloid sarcoma is a rare extramedullary manifestation of leukemia that consists of immature cells of the granulocytic series [1]. Although myeloid sarcoma can involve any ocular tissue, a myeloid sarcoma in the eyelid is less common [2, 3]. Ocular myeloid sarcomas may appear at any time during the course of acute myeloid leukemia [3, 4], and they often develop simultaneously with acute myeloid leukemia during onset or relapse [1, 4]. In contrast, an ocular myeloid sarcoma that develops during chemotherapy is extremely rare, with only one reported case with an intraocular lesion [5].

In this case report, we present a case of a myeloid sarcoma in the upper eyelid that developed during chemotherapy for acute myeloid leukemia.

Case Report

The Institutional Review Board (IRB) of the Ethics Committee of Aichi Medical University approved this retrospective case report (2015-012), which adhered to the tenets of the 1964 Declaration of Helsinki. As the IRB requested us to obtain informed consent from the patient or a patient's kin before the collection of data for this retrospective case report, informed consent was obtained from the brother due to the patient's death. Informed consent was also obtained from the brother for the publication of this case report and any accompanying images.

An 80-year-old female was diagnosed with myelodysplastic syndrome 1 year before referral to our clinic. She underwent erythrocyte transfusion therapy for severe anemia. As the myelodysplastic syndrome progressed to acute myeloid leukemia 3 months after the initial diagnosis, she was administered two cycles of low-dose cytarabine (20 mg/m²/day) and aclarubicin hydrochloride (14 mg/m²/day) chemotherapy [6], followed by azacitidine injections (1 cycle, 75 mg/m²/day × 7 days). As the patient showed a hypocellular marrow, cytarabine and aclarubicin hydrochloride were administered for 5 (recommended medication days, 14 days) and 3 days (recommended medication days, 4 days), respectively, in each cycle of the chemotherapy for preventing a delayed recovery of a normal blood count after the chemotherapy. The interval between the cycles was approximately 4 weeks. As acute myeloid leukemia recurred immediately after the fourth cycle of the azacitidine injections, cytarabine (1 cycle, 20 mg/m²/day × 10 days), aclarubicin hydrochloride (1 cycle, 14 mg/m²/day × 3 days), and granulocyte colony-stimulating factor (granisetron hydrochloride; 1 cycle, 200 μg/m²/day × 10 days) (CAG) chemotherapy was started [6]. Between the second and third cycles of CAG chemotherapy, the patient noticed an eyelid mass with the size decreasing during the 3 cycles of CAG chemotherapy.

Upon the first examination after the 3 cycles of the CAG chemotherapy, an elastic, hard, pinkish, relatively smooth surface mass was observed in the left upper eyelid margin without madarosis (fig. 1). Systemic computed tomography did not reveal any other lesions. We then performed a biopsy under local anesthesia. The pathological examination revealed a proliferation and an infiltration of tumor cells, with a high nuclear/cytoplasmic ratio (fig. 2). Apoptosis and mitosis were observed in the lesion. Immunostaining was positive for cluster of differentiation (CD) 68 and CD117, but negative for CD34, terminal deoxynucleotidyl transferase, cytokeratin (AE1/AE3), and cytokeratin-20. The pathological diagnosis was myeloid sarcoma.

Due to the poor systemic condition of the patient and since no blast cells were shown in the peripheral blood at the time of the biopsy, she subsequently received azacitidine injections without an additional cycle of CAG chemotherapy. The residual eyelid tumor decreased in size at 3 months following the biopsy, when the course of the azacitidine injections was completed. However, acute myeloid leukemia recurred, and she died 5 months after her first examination.

Discussion

This is the first reported case of an eyelid myeloid sarcoma that developed during chemotherapy for acute myeloid leukemia. Although no blast cells were shown in the peripheral blood at the time of the biopsy, acute myeloid leukemia recurred, and the patient died. An eyelid myeloid sarcoma may be a sign of an incomplete remission of acute myeloid leukemia despite effective chemotherapy and poor prognosis [4].

The patient suffered from myelodysplastic syndrome before the onset of acute myeloid leukemia, which is one of the risk factors for developing acute myeloid leukemia. In cases with preexisting myelodysplastic syndrome, chemotherapy tends to be less effective for acute myeloid leukemia [7], possibly resulting in the development of an eyelid myeloid sarcoma, as it occurred in this patient.

The mass was elastic, hard, and pinkish, with a relatively smooth surface, but without madarosis. This appearance was different from other eyelid myeloid sarcomas described in previous reports that showed multiple erythematous lesions of varying sizes [8, 9]. In contrast, it was similar in appearance to malignant lymphomas [10] and Merkel cell carcinomas [11]. It may be difficult to diagnose similar masses that develop before the onset of acute myeloid leukemia [3, 10], although the patient described in this case report had a history of acute myeloid leukemia. Ophthalmologists and pathologists, therefore, need to know the variations in the appearance of eyelid myeloid sarcomas.

In conclusion, we report the first case of an eyelid myeloid sarcoma that developed during chemotherapy for acute myeloid leukemia. An eyelid myeloid sarcoma may be a sign of incomplete remission of acute myeloid leukemia during effective chemotherapy and poor prognosis.

Statement of Ethics

The Institutional Review Board (IRB) of the Ethics Committee of Aichi Medical University approved this retrospective case report (2015-012), which adhered to the tenets of the 1964 Declaration of Helsinki. As the IRB requested us to obtain informed consent from the patient or a patient's kin before the collection of data for this retrospective case report, informed consent was obtained from the brother due to the patient's death. Informed consent was also obtained from the brother for the publication of this case report and any accompanying images.

Disclosure Statement

The authors have no competing interests to declare.