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Pheochromocytoma With Langerhans Cell Histiocytosis: A Rare Tumor-in-Tumor Case
Cheng Lei1, Yulong Guo2, Yixin Luo3
1Department of Pathology The Second Xiangya Hospital, Central South University Changsha China.
Clinical Case Reports
|March 2, 2026
Abstract:
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.

