Myeloblastic meningeal neoplasm: an unusual natural history.
Saranya B GomathyAanchal KakkarRitu GuptaArunmozhimaran ElavarasiPublished in: BMJ case reports (2024)
Myeloid sarcoma is a very rare extramedullary malignant tumour, most often associated with acute myeloid leukaemia. We report the case of a man in his early 20s who presented with chronic headache, raised intracranial pressure and progressive vision loss of 2 years duration with no systemic manifestations. He had a history of myeloid sarcoma of the left thigh 15 years ago, treated with external beam radiotherapy and in complete remission for more than 13 years. However, the progressive blindness remained unexplained for 2 years, and he was eventually diagnosed with isolated meningeal relapse without marrow or systemic involvement. Imaging revealed subarachnoid haemorrhage, diffuse leptomeningeal enhancement and involvement of lower dorsal cord and conus, and cerebrospinal fluid cytology showed myeloid blasts. He was managed with intrathecal chemotherapy and craniospinal irradiation, after which he had mild improvement in vision.
Keyphrases
- cerebrospinal fluid
- bone marrow
- dendritic cells
- acute myeloid leukemia
- multiple sclerosis
- drug induced
- early stage
- small cell lung cancer
- spinal cord
- low grade
- locally advanced
- radiation therapy
- squamous cell carcinoma
- liver failure
- systemic lupus erythematosus
- respiratory failure
- high grade
- radiation induced
- mass spectrometry
- ultrasound guided
- newly diagnosed
- photodynamic therapy
- fine needle aspiration
- rectal cancer
- free survival
- chemotherapy induced