Spontaneous Resolution of Primary Hypercortisolism of Cushing Disease After Pituitary Hemorrhage
ABSTRACT: Objective: To describe a case of spontaneous resolution of primary hypercortisolism from Cushing disease (CD) due to pituitary apoplexy (PA). Methods: Clinical, laboratory, and pathologic information are described. Results: A 59-year-old female presented with a headache, a 2.3 cm sellar m...
| Main Authors: | , , |
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| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2020-01-01
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| Series: | AACE Clinical Case Reports |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2376060520300687 |