Rare Case of Mediastinal Myeloid Sarcoma
Myeloid sarcoma is a rare tumor mass with extra medullary growth pattern, composed of myeloblast or immature myeloid cells. Myeloid sarcoma (MS) is a distinct clinical presentation of acute myeloid leukemia (AML) where less than 1% of patients present with prominent extra medullary disease which most commonly involves the bone, skin, lymph node, soft tissues, gastrointestinal tract or testes. The recommended treatment regimen in isolated myeloid sarcoma or with bone marrow involvement is upfront systemic chemotherapy. We report a case of a young female with anterior mediastinal mass diagnosed as myeloid sarcoma which was refractory to chemotherapy.
Myeloid sarcoma (MS) also called granulocytic sarcoma (GS), myeloblastoma, or chloroma may present simultaneously with or precede bone marrow disease. Typically, myeloid sarcoma may develop as part of acute myeloid leukemia (AML), myeloproliferative neoplasm, myelodysplastic syndrome or it may manifest at relapse, especially in patients following allogenic hematopoietic stem cell transplant [1-3]. As per WHO definition, the tumor itself consists of myeloid blast with or without maturation occurring at an anatomic site other than the bone marrow . The clinical and pathological diagnosis of MS can be highly challenging. The European Society for Hematology recognizes variety of extramedullary manifestation of myeloid neoplasm:
1) MS with concurrent AML; 2) extramedulllary relapse of AML; 3) blast phase/transformation of myeloprolifrative neoplasm; and 4) isolated MS . Isolated MS is a rare entity and has also distinct clinical presentation, reflecting variation in the location and size of MS lesions and most commonly involves the bone, skin, lymph node, soft tissues, gastrointestinal tract and testes.
We are discussing a rare presentation of MS located at unusual anatomical site i.e. anterior mediastinum with poor response to standard treatment.
A 25-year-old female presented with history of shortness of breath associated with chest pain, fever, and weight loss for two months. On presentation she was dyspneic. Initial laboratory investigations showed hemoglobin of 11 g/dL, platelet count, 533 × 109/L and white blood cell count (WBC) of 22 × 109/L with differential count of 82 % neutrophils, 10 % lymphocytes, 7 % monocytes, 1 % eosinophils and normal RBC indices. Achest X-ray was done which revealed left sided moderate effusion and right sided mild effusion with mediastinal widening (Figure 1).
Subsequently, contrast enhanced CT chest, abdomen and pelvis was done which showed, anterior mediastinal heterogeneous soft tissue lesion abutting and displacing the major mediastinal vessels, measuring approximately 95 x 37 x 74 mm in transverse, anteroposterior, and craniocaudal dimensions respectively. (Figure 2).
Concomitantly, there was presence of pulmonary embolism involving subsegmental branches of right lower pulmonary artery with right sided pleural effusion and left sided loculated effusion (Figure 1). After discussion in multidisciplinary case discussion meeting, it was recommended to perform pleural fluid drainage followed by left sided video-assisted thoracoscopic surgery (VATS) for decortication and biopsy of mediastinal mass. The patient received broad spectrum antibiotics along with therapeutic anticoagulation with insertion of bilateral chest tubes. Morphologically, the mediastinal mass biopsy showed presence of sheets of neoplastic cells which were pleomorphic, with vesicular nuclei, variably prominent nucleoli and abundant eosinophilic to clear cytoplasm (Figure 3).
Immunohistochemistry stained positive for myeloperoxidase (MPO), CD-79a and CD-43 while it was negative for CD3, CD-20, PAX-5, CD-23, CD-117, CD-68, CD-30 and CD34. Considering her diagnosis bone marrow biopsy and immunophenotyping by flowcytometry of pleural fluid was done which showed no involvement with blast cells. Therefore, she was labelled as a case of primary myeloid sarcoma.
She received induction chemotherapy with 3+7 regimen i.e., Daunorubicin 50mg/m2 (3 days) and Cytarabine 100 mg/m2 (7 days). Her subsequent radiological scans showed no significant improvement, indicative of refractory/resistant disease (Figure 4).
Clinically, her condition worsened as she remained on continuous non-invasive ventilation support (bilevel positive airway pressure – BiPAP) for persistent tachycardia and tachypnea which was secondary to worsening pleural effusion and bronchopneumonia. After expert consultation with the cardiothoracic team, she underwent repeat right sided VATS and decortication for loculated pleural effusion.
Considering chemo resistant disease, radiation oncology was consulted for treatment and was offered radiation therapy on urgent basis with initial 2D (2 dimensional) technique (Figure 5).
After 2 fractions of radiation therapy her clinical condition improved significantly (BiPAP support was discontinued) so it was proposed to switch her to CT Based 3D (3 dimensional) conformal radiation therapy which shows a response to initial two fractions of radaition therapy (Figure 6 and 7).
She completed 10 fractions at 3 Gray per fraction over two weeks with cumulative dose of 30 Gray. Eventually, she was discharged from in-patient services in a stable condition and without NIV support.
Four weeks after discharge, her follow up contrast enhanced CT scan of chest, abdomen and pelvis showed further reduction in the size of anterior mediastinal mass, however there was development of pleural thickening along the left crus of the diaphragm and few retroperitoneal nodes. Subsequently, PET/CT scan after two weeks showed further reduction in size and FDG uptake of anterior mediastinal mass (Figure 8). She was then planned for systemic second line chemotherapy.
She was then planned for systemic second line chemotherapy.
As isolated myeloid sarcoma is a very rare entity frequently resembling lymphoma in clinical presentation. It poses a major diagnostic challenge for both pathologists and clinicians. We report a similar case of a 25-year- old female who was diagnosed as myeloid sarcoma on anterior mediastinal mass. Mediastinal primary myeloid sarcoma (MS) is extremely rare and only few case reports have been published in literature. This entity has a high rate of misdiagnosis. i.e., 46% and is misdiagnosed as lymphoma . Immunohistochemical detection of intracellular myeloperoxidase (MPO), a major constituent of primary granules of neutrophilic myeloid cells, confirms a diagnosis of MS. The diagnosis is based on immunohistochemical stains which include CD13 and CD68 (markers for granular monocytic and macrophagic cells), MPO and CD117 (markers for myeloid differentiation), lysozyme marker for monocytic lineage, CD43 (marker for myeloid cells, T and B cells), and CD34 and terminal deoxynucleotidyl transferase (TdT) (markers for immature cells) . In our patient’s case, immunohistochemical evaluation revealed strong positivity of MPO and CD43. Due to limited prospective trials, treatment strategies for MS are not well established but because most of patients with isolated MS progress to AML, systemic chemotherapy is recommended treatment of choice followed by consolidation similar to AML . Retrospective series have demonstrated that isolated MS treated with local radiotherapy alone has a high rate of progression to AML and a short no leukemic interval [9, 10]. The use of radiotherapy is also not well studied as a prospective means of treatment of MS but can produce excellent, durable local control at the targeted site; however, it is also an inadequate treatment option unless used in combination with systemic chemotherapy .
A series of 21 patients with isolated MS demonstrated that disease recurrence was lower in a group that received chemo-radiotherapy than those receiving radiotherapy alone . Another retrospective series that included 90 patients also demonstrated that, local radiotherapy had no effect on overall survival. Hematopoietic stem cell transplantation (HSCT) also used, retrospectively, in MS patients, reported data showed an advantage of both auto or allo-HSCT in MS patients with or without concomitant AML irrespective of age, gender, anatomic location clinical presentation or cytogenetic status [8, 10, 13]. Our patient did not respond to standard systemic chemotherapy, but she showed excellent reduction of mediastinal mass after low dose radiotherapy. According to literature, radiation therapy for the MS is effective to achieve response but it does not improve the disease-free interval and the overall survival. Therefore, chemotherapy is recommended even with initial response to radiation similar to the treatment of acute myeloid leukemia . This patient has been planned for systemic chemotherapy followed by allogenic stem cell transplant.
In Conclusion, myeloid sarcoma is a rare entity and lacks standardized treatment protocols. Our patient with anterior mediastinal mass diagnosed as MS who was chemo-refractory but responded to radiation therapy, way forward will be to treat her with systemic chemotherapy followed by allogeneic stem cell transplant.
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