Alveolar granulocytic sarcoma of the mandible in a patient with HIV
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Nataša Colović1, Vladimir Jurišić, Tatjana Terzić
1Institute of Hematology, Clinical Center of Serbia, Belgrade, Serbia.
Insights
Granulocytic sarcoma, a rare cancer, appeared in an HIV-positive patient. This case highlights the rarity of granulocytic sarcoma in individuals with human immunodeficiency virus (HIV).
Area of Science:
- Oncology
- Hematology
- Infectious Diseases
Background:
- Granulocytic sarcoma (chloroma) is a rare extramedullary tumor primarily associated with acute myelogenous leukemia and other myeloproliferative neoplasms.
- While typically seen in leukemia patients, its occurrence in individuals with human immunodeficiency virus (HIV) is exceptionally rare.
Observation:
- A case report details a 52-year-old HIV-positive female with a CD4+ count of 321 cells/ml who developed an alveolar granulocytic sarcoma of the mandible.
- Pathological analysis revealed immature cells positive for myeloid markers (CD13, CD33, CD15, CD11b, CD64) and negative for stem cell markers (CD34, CD117, HLA-DR).
Findings:
- The patient achieved complete remission after a week of chemotherapy but later developed a second granulocytic sarcoma.
- Recurrence coincided with a severe decline in CD4+ count (3 cells/ml) and Th/Ts index inversion, preceding death from gram-negative sepsis.
Implications:
- This case underscores the extreme rarity of granulocytic sarcoma in the context of HIV infection.
- It highlights the potential for aggressive disease progression and poor outcomes in advanced HIV, particularly with opportunistic infections like sepsis.
Background:
Granulocytic sarcoma (chloroma) occurs primarily in patients with acute myelogenous leukemia although it can also appear in connection with other myeloproliferative disorders.
Case Report:
We present the case of a 52-year-old human immunodeficiency virus (HIV)-positive female patient with a CD4+ count of 321 cells/ml, who developed an alveolar granulocytic sarcoma of the mandible. Pathological analysis of the tumor mass showed an infiltrate of immature cells which were positive for CD13, CD33, CD15, CD11b, and CD64, and negative for CD34, CD117, and HLA-DR. The patient achieved complete remission following a 1-week course of chemotherapy, however, 7 months later she developed a second granulocytic sarcoma in the left soleus muscle. The absolute CD4+ count had now reduced to 3 cells/ml with an inversion in the Th/Ts index (0.01), and she died of gram-negative sepsis 1 month later.
Conclusions:
Granulocytic sarcoma is extremely rare in patients with HIV. The case is discussed with reference to the literature.
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