Granulocytic sarcoma also known as chloroma or extramedullary myeloid tumor is a collection of leukemic cells outside the bone marrow. These tumors occur in 3–8% of acute nonlymphoid leukemia. The common sites affected by it are skin, lymph nodes, central nervous system, and reproductive organs. Involvement of gastrointestinal tract is relatively rare with small bowel being the commonest site.

We report a case of gastric myeloid sarcoma in a young female at 17 weeks of gestation presenting with dysphagia, epigastric pain, and vomiting.

A 25-year-old woman with 17 weeks of gestation (G3P2) presented with progressive dysphagia, epigastric discomfort, persistent postprandial vomiting, and weight loss for one month. Initial investigations were within normal limits. Upper GI endoscopy showed thickened nodular friable mucosa at cardia of stomach extending into the posterior wall (Figure 1). Multiple deep biopsies from gastric cardia showed normal mucosal glands with expansion of lamina propria by infiltrates of atypical cells, intermixed with granulocytic precursor cells (Figure 2). Immunohistochemistry panel showed that the cells were negative for CD20, CD5, CD3, CD10, and cytokeratin markers, with intense positivity for immature myeloid markers (myeloperoxidase, CD34, and CD117) (Figure 3), consistent with granulocytic sarcoma of the stomach. A week later she developed fever with WBC count of 34,800 cells per cu mm. A bone marrow biopsy (Figure 4) and flow cytometry analysis showed features consistent with acute myeloid leukemia (AML-M4) with blast count of 77%. Pregnancy was terminated.

Granulocytic sarcoma is a rare malignant solid tumor composed of primitive precursors of the granulocytes deposited outside the bone marrow. It was called “chloroma” due to its green color. Rappaport renamed it “granulocytic sarcoma” because the color varied depending on the concentration of the pigmented enzyme (myeloperoxidase). It is more common in children than adults and often occurs concurrently with AML. They rarely present with relapse of leukemia, in blast crisis of myeloproliferative disorder, as leukemic transformation in myelodysplastic syndrome [¹]. Granulocytic sarcoma in the Gastrointestinal (GI) tract arises from nests of hematopoietic cells [²]. The commonest site of involvement is small bowel [³] followed by colon, appendix, biliary tract, and stomach [⁴].

The endoscopy findings can vary from normal to mucosal nodularity or mass lesions. It may precede hematologic leukemia by months or years [⁵]. Tissue biopsies, bone marrow biopsy, immunohistochemistry, and cytogenetics assist to diagnose chloroma. It is common in patients with M2, M4, or M5 class of French-American British (FAB) classification.

Systemic intensive chemotherapy is the first line of treatment [⁶]. Our patient is taking chemotherapy and is doing well on followup. This subject was different from other reported cases of gastric chloroma. She presented with dysphagia in pregnancy and the diagnosis of gastric chloroma preceded the detection of AML involving peripheral blood and bone marrow. To our knowledge, this is the first case of the AML presenting as sarcoma of stomach in pregnancy. Involvement of cardia of stomach has also not been reported earlier.

The authors declare that they have no competing interests or financial gain.