Pheochromocytoma With Langerhans Cell Histiocytosis: A Rare Tumor‐in‐Tumor Case
Langerhans cell histiocytosis (LCH) occurring in a Pheochromocytoma in the adrenal gland is exceptionally rare and prone to misdiagnosis. The special coexistent tumors harbor distinct genetic mutations. This uncommon case could introduce novel considerations and a strong teaching message to all the clinicians and pathologists.
Authors
- Luo Jiadi
- Yixin Luo
- Qingchun Liang
- Cheng Lei
- Yulong Guo
Institutions
- Central South University (CN)
- Second Xiangya Hospital of Central South University (CN)
- Anyang Hospital of Traditional Chinese Medicine (CN)
Publication Details
- Journal
- Clinical Case Reports
- Published
- 2026-02-26
- DOI
- https://doi.org/10.1002/ccr3.72185
- Primary Topic
- Histiocytic Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 0.00