Abstract
Myeloid sarcoma (MS) is a rare, extramedullary tumor consisting of immature white blood cells of myeloid lineage. MS is usually associated with the concurrent diagnosis of acute myeloid leukemia (AML) but can also present in the absence of bone marrow disease or at relapse of AML. MS of the gynecologic tract is exceedingly rare; however, it is hypothesized that it is likely more prevalent than previously understood given postmortem findings and persistence in preserved ovarian tissue. There is minimal literature surrounding MS and extramedullary relapse with no clear guidelines. This is a case report of a 48-year-old woman with MS involving the uterine corpus, fallopian tubes, and left ovary followed by a literature review. The overall aim is to review data regarding leukemic immune evasion and sanctuary sites in order to raise awareness as this represents an important and underrecognized hematologic malignancy in an often misdiagnosed, underrecognized site.
1. Introduction
Myeloid sarcoma (MS) is a rare, extramedullary tumor consisting of immature white blood cells of myeloid lineage that disrupt the tissue architecture in which it invades. MS has been reported in 2-8% of patients with acute myeloid leukemia (AML) and is most commonly diagnosed concurrently with this disease [1]. Rarely, MS presents as the initial manifestation of AML or proceeds AML relapse. Myeloid sarcoma can occur in the absence of bone marrow disease, which is known as isolated or nonleukemic MS. Although MS is most commonly found in soft tissues, bone, lymph nodes, the central nervous system, testicles, and ovaries, there are rare reports of the involvement of the uterus and fallopian tubes [2]. It is widely believed that the gynecologic tract may be an important and underrecognized reservoir of leukemic blasts through immune evasion, resulting in an increased risk of disease relapse.
2. Case Report
A 48-year-old woman (gravida 1, para 1) with a history of polycystic ovarian syndrome and thyroid cancer treated with radioactive iodine presented to her endocrinologist for follow-up and was found to have an elevated testosterone level. An ultrasound of the pelvis showed enlarged ovaries that were hypoechoic with increased vascularity concerning for a neoplasm (Figures 1(a) and 1(b)). To further evaluate the radiographic findings, the patient was scheduled for laparoscopic bilateral salpingo-oophorectomy (BSO). A complete blood count (CBC) during her presurgical appointment was notable for pancytopenia. The patient was sent for hematology for evaluation. A bone marrow biopsy was performed that showed AML with replacement of the bone marrow by blasts, which by flow cytometry of the bone marrow aspirate were found to express myeloperoxidase (MPO), HLA-DR, dim CD123, CD4, and CD56, but lacked CD34 and CD117. Immunostaining of the bone marrow core biopsy showed similar findings except the blasts were dim MPO-positive and were positive for CD68 (KP1). Cytogenetics showed an abnormal hyperdiploid karyotype with three related clones. Abnormalities included extra copies of chromosome 6, 20, 21, and 22 and included an interstitial deletion of 8q. A myeloid molecular panel, covering 40 genes, showed no mutations. The patient was treated with standard induction chemotherapy (idarubicin and cytarabine). The patient achieved clinical remission, the bone marrow biopsy showed no morphologic or immunophenotypic evidence of residual disease, and cytogenetics showed a normal karyotype. The patient underwent workup for an allogeneic bone marrow transplant, which included, in light of her previous laboratory studies, repeat testing of a serum testosterone level. Her testosterone level was elevated which again led to an ovarian ultrasound that showed findings similar to the first examination. Based on these studies, there was concern for bilateral stromal ovarian tumors. The previously planned laparoscopic BSO was performed. The patient was then admitted to the transplant service to begin transplant conditioning.
(a)
(b)
(c)
(d)
The bilateral ovaries and fallopian tubes showed no abnormalities on gross visual examination. Histologic examination, however, showed an atypical mononuclear cell infiltrate in both fallopian tubes and focally within the left ovary. Immunoperoxidase staining of paraffin tissue sections showed that these mononuclear cells expressed HLA-DR, CD33, CD56, KP1 (CD68), CD123, and dim focal MPO but were negative for CD34 and CD117, an immunophenotypic profile identical to that of the patient’s previously diagnosed AML (Figures 2(a)–2(f)). Thus, the findings were consistent with myeloid sarcoma involving the fallopian tubes and ovary. Additional histologic findings showed bilateral ovarian stromal hyperplasia, hyperthecosis, and a microscopic granulosa cell tumor (2 mm), findings consistent with her clinical hyperandrogenism.
(a)
(b)
(c)
(d)
(e)
(f)
(g)
(h)
Following surgical resection and a pathologic review, the patient’s testosterone levels decreased precipitously and a repeat bone marrow biopsy was performed, which showed recurrent AML. The plan for the patient to undergo an allogeneic bone marrow transplant was aborted.
The patient underwent salvage reinduction with high-dose cytarabine and gemtuzumab. A repeat bone marrow biopsy following treatment when the patient was in clinical remission showed no morphologic evidence of disease but showed minimal residual disease based on flow cytometry (0.32% abnormal blasts identified). Approximately two weeks later, the patient began experiencing abnormal uterine bleeding in the setting of worsening thrombocytopenia. Imaging showed an enlarged, heterogeneous uterus with multifocal hypodense and cystic foci (Figure 1(c)). The patient had an endometrial biopsy to determine if this represented leukemic infiltration, a solid tumor malignancy, or other pathology.
The biopsy contained small fragments of endometrium with an atypical mononuclear cell infiltrate. The cells expressed CD56 and HLA-DR, consistent with MS (Figures 2(g) and 2(h)). A concurrent bone marrow biopsy revealed a hypercellular marrow with increased blasts (~10% by immunohistochemistry), consistent with persistent AML. She then reported new-onset hematochezia; a CT scan demonstrated a 2.2 cm enhancing, likely a centrally necrotic lesion in the jejunum representing further extramedullary disease (Figure 1(d)). The patient’s clinical status began to rapidly decline with constant rectal and vaginal bleeding. Two months after the diagnosis of relapse, the patient died from cardiopulmonary arrest secondary to disease.
3. Discussion
This demonstrates a rare, interesting case of AML diagnosed during the evaluation for known bilateral adnexal masses. Following surgery, she was then found to have myeloid sarcoma of the fallopian tubes and the left ovary with additional findings of bilateral ovarian stromal hyperplasia, hyperthecosis, and a microscopic granulosa cell tumor. Shortly after recurrence of her AML, the patient began experiencing abnormal uterine bleeding in the setting of myeloid sarcoma now with uterine involvement and rapid clinical decline. This case further exemplifies the aggressive nature of myeloid sarcoma after multiple chemotherapy regimens as well as a clear predilection for the gynecologic tract among certain cancer types.
Extramedullary tumors of myeloid cells were first described in the literature by British physician Allan Burns in 1811 [3]. They were later referred to as chloromas by King in 1853, derived from the Greek word chloros (green), because of the green-tinged color of these tumors due to the presence of myeloperoxidase (MPO) [4]. Nearly six decades later, Dock and Warthin recognized the connection between “chloromas,” i.e. myeloid sarcomas, and acute leukemia [5]. As these tumors became better understood over time, the term “granulocytic sarcoma,” coined by Rappaport in 1967, was used to describe any extramedullary manifestation of AML [6]. In 2008, the World Health Organization (WHO) classified the definition of MS as “a tumor mass consisting of myeloid blasts with or without maturation occurring at an anatomic site other than the bone marrow.” [7] As per the 2017 update of the WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues, “myeloid sarcoma” is the current correct terminology for these extramedullary myeloid tumors [8].
The pathogenesis of female reproductive organ involvement with MS is not fully understood. Neural cell adhesion molecule (NCAM; CD56), which is present in normal ovarian, testicular, and gastrointestinal tissue, is believed to play a role in the homing of MS to specific tissues [9]. Additionally, reproductive organs have inherent barriers, which are hypothesized to serve as sanctuary sites for leukemic cells to proliferate despite systemic therapy [10]. Literature has shown that once a single focus of extramedullary disease is identified, progression in other organs as well as the bone marrow usually follows within a year [11]. Furthermore, this case shows that complete bone marrow response may not signify that sanctuary sites, like the ovaries, are free of disease.
The clinical and pathologic diagnosis of MS has been challenging historically. MS most commonly occurs concurrently with AML with an estimated incidence between 2.5 and 9.1% of patients [12]. However, primary (isolated) MS occurring outside of AML is exceedingly rare with reported rates as low as two cases per million adults. Isolated MS can differ from concurrent disease as regards tumor behavior, effectiveness of treatment, and prognosis. Given the diversity of MS presentations and locations, as well as low clinical suspicion, this disease commonly goes misdiagnosed [12]. Meis et al. reported a misdiagnosis rate of MS as high as 75% in a 1986 retrospective series [13]. More recent reports now demonstrate that nearly 25-50% of all patients with MS will go misdiagnosed [12, 14]. The most common reason cited for misdiagnoses has been inadequate immunophenotyping of the MS lesion [15]. Immunohistochemical staining is important in the correct diagnosis, as MS lesions express both myeloid and monocytoid antigens including CD45, CD43, and CD15 [16].
There has been scarce literature investigating the survival and prognosis of patients with MS. First-line treatment usually involves systemic induction chemotherapy as surgical excision does not delay spread of disease or improve prognosis [16, 17]. There have also been case reports that suggest that a robust inflammatory response following a surgical procedure could worsen MS or lead to a postoperative persistent febrile syndrome [18].
MS most commonly manifests in the skin, subcutaneous tissues, and the lymph nodes. Claerhout et al. conducted a case series of 41 patients with de novo MS and 31 patients with secondary disease [19]. Among both cohorts, respectively, they found that MS localized to the skin in 24-25.5% of cases, lymph nodes (18.2-16.0%), gastrointestinal tract [20] (10.9-2.0%), breast (7.3-10.0%), ovary (3.6-0.0%), cervix/urine corpus (1.8-4.0%), bone (3.6-6.0%), and brain (3.6-6.0%). There have also been reports of MS invading into the vulva. Although MS of the gynecologic tract is exceedingly rare, it is hypothesized that it may actually be underdiagnosed based on postmortem studies showing frequent gynecologic involvement in women who have died of myeloid leukemia [21, 22].
This case report is consistent with previous rare literature reports and adds to the current literature. One of the largest previous reported series of MS involving the gynecologic tract, Garcia et al. reported a series of 11 cases at a single center case series from 2006 spanning the previous 31 years [2]. Among gynecologic organs, the uterus was the most frequent site of disease—involved in 8 patients. Myeloid sarcoma was confined to the ovary in 2 patients, involved the fallopian tubes in 2 patients, and was confined to the clitoris in 1 patient. Four of the patients exhibited concurrent involvement of multiple gynecologic sites. Other studies have described cases with multisite involvement in the gynecologic tract, including one with disease in the cervix, mesosalpinx, and ovaries. In addition, cases with disease concurrently involving the gynecologic tract and extragynecologic sites have also been reported [22].
4. Conclusion
In conclusion, myeloid sarcoma of the gynecologic tract represents an important and often misdiagnosed hematologic malignancy in an underrecognized site. As this paper has demonstrated, MS in the setting of AML and extramedullary relapse is exceedingly rare; however, it likely occurs more than previously understood, especially given the postmortem findings and persistence in preserved ovarian tissue. Physicians should have an increased awareness regarding this potential site of disease with a high index of suspicion. As immunophenotyping is the primary cause of misdiagnosis, appropriate tissue with immunohistochemical staining is important. Additional studies are necessary to better understand this rare manifestation, and in turn allowing for better understanding of myeloid malignancies in general as well.
Conflicts of Interest
The authors declare that there is no conflict of interest regarding the publication of this paper.