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Published on: January 17, 2018
Pineal Diffuse Large B-Cell Lymphoma Concomitant With Pituitary Prolactinoma: Possible Correlation Between 2
Yeong-Jin Kim1, Hee Kyung Kim, Deok-Hwan Yang
1From the Department of Neurosurgery (Y-JK, SJ, K-SM); Department of Internal Medicine (HKK, D-HY); and Departments of Pathology, Chonnam National University Research Institute of Medical Sciences (M-GN, J-HL, K-HL), Chonnam National University Hwasun Hospital and Medical School, Hwasun-gun, Jeollanamdo, South Korea.
This case report details a rare instance of pineal gland lymphoma co-occurring with a prolactin-producing pituitary adenoma. The patient presented with Parinaud syndrome and was diagnosed with diffuse large B-cell lymphoma (DLBCL).
Area of Science:
- Neuro-oncology
- Endocrinology
- Pathology
Background:
- Pineal gland tumors are rare and can present with diverse neurological symptoms.
- Pituitary adenomas, particularly prolactinomas, are common endocrine tumors.
- The simultaneous occurrence of these two distinct tumors is exceptionally uncommon.
Observation:
- A 51-year-old male presented with headaches, nausea, diplopia, and memory loss.
- Clinical examination revealed Parinaud syndrome (impaired upward gaze and convergence).
- MRI showed a pineal mass and an enlarged sella with a coexisting mass, alongside hyperprolactinemia.
Findings:
- Surgical removal of the pineal mass confirmed diffuse large B-cell lymphoma (DLBCL).
- The lymphoma was secondary to a primary gastric tumor.
- The patient also had a prolactin-producing pituitary adenoma.
Implications:
- This case highlights the importance of comprehensive evaluation for concurrent pathologies in patients with complex presentations.
- The potential role of hyperprolactinemia in lymphoma progression warrants further investigation.
- Understanding rare tumor co-occurrences can improve diagnostic and therapeutic strategies.
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