ArticleFrontiers in endocrinology2021
Primary Adrenal Lymphoma: Two Case Series From China.
Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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Who cites it
12 citing papers in PubMed, 11 citations in OpenAlex.
- Article
- Adrenal lymphoma with hypertension: A report of three cases.Oncology letters · 2026Article
- Unilateral primary adrenal high-grade B-cell lymphoma treated with R-CHOP chemotherapy: a case report and literature review.BMC urology · 2026Review
- Bilateral Adrenal Metastases From Breast Cancer 14 Years After Remission: Diagnostic Value of "Adrenal Thickening".JCEM case reports · 2026Article
- Non-Hodgkin's lymphoma presenting as a retroperitoneal mass in the emergency department: a case report.Frontiers in medicine · 2026Article
- Bilateral adrenal masses and adrenal insufficiency: a rare case of primary adrenal lymphoma.Endocrinology, diabetes & metabolism case reports · 2026Article
- Primary Adrenal Lymphoma Diagnosed by Endoscopic Ultrasound Fine-Needle Aspiration Biopsy: A Case Report.The American journal of case reports · 2025Article
- Primary adrenal lymphoma and its mimics: clinico-radiological differential diagnosis.Frontiers in endocrinology · 2025Article
- Papillary thyroid carcinoma: ≤ 10 mm does not always mean pN0. A multicentric real-world study.Updates in surgery · 2024Article
- Article
- Addison's Disease: Diagnosis and Management Strategies.International journal of general medicine · 2023Review
- Analysis of characteristics of four patients with adrenal unicentric Castleman disease.Frontiers in endocrinology · 2023Article
Corrections and comments
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Authors and funding
10 authors at 3 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objective: Primary adrenal lymphoma (PAL) is a rare form of adrenal mass. We summarize our experience in its clinical presentation, biochemical indexes, radiological features, pathological information, therapy regimens, and outcomes. Methods: This was an institutional review board-approved retrospective review of medical records and surgical pathology specimens of patients with a diagnosis of PAL at the Chinese People's Liberation Army General Hospital and the First Affiliate Hospital of Xiamen University between July 2007 and July 2017. Results: Twenty-six patients were identified. The mean age at presentation was 60.84 ± 13.14 years with a male-to-female ratio of 2.25:1 (18:8). The most common presenting symptoms were loss of appetite (65%, 17/26), weight loss (62%, 16/26), abdominal pain (58%, 15/26), and fatigue (58%, 15/26). The levels of lactate dehydrogenase (75%, 15/20), β Conclusion: PAL is a rare disease. The clinical characteristics of PAL include loss of appetite and weight loss. Endocrine evaluation should be performed to determine whether patients have adrenal insufficiency, especially patients with bilateral lesions. FDG-PET appears to be more accurate than other imaging modalities in revealing extra-adrenal sites. Better therapy is required to improve the poor prognosis of PAL.
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