| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
EXTENSIVE CLINICAL EXPERIENCE |
Departments of Neurological Surgery (N.P., D.M.P., J.J., E.R.L.) and Pathology (M.B.L.), Division of Neuropathology, and Department of Medicine (M.L.V.), Division of Endocrinology, University of Virginia, Charlottesville, Virginia 22903
Address all correspondence and requests for reprints to: Nader Pouratian, M.D., Ph.D., Resident, Department of Neurological Surgery, University of Virginia, Box 800212, Charlottesville, Virginia 22903. E-mail: np5k{at}virginia.edu.
Context: Despite the success of transsphenoidal surgery (TSS) for the treatment of Cushings disease, in a number of cases, an ACTH-staining pituitary adenoma is not identified histologically. The clinical significance of lack of histological confirmation remains unclear.
Setting: This was a retrospective review of patients treated at the University of Virginia Medical Center.
Patients: Of 490 TSS procedures for Cushings disease between 1993 and 2004, we identified 111 cases without histological adenoma confirmation.
Main Outcome Measure: Remission and recurrence of Cushings disease were measured.
Results: Overall, 50% of these patients achieved remission, a figure lower than for our entire series (79%) and for patients with histological confirmation of an ACTH-staining adenoma (88%) (P < 0.001). Patients with a history of two prior TSS achieved remission less often than patients with a history of fewer TSS (P = 0.026). No other factors influenced remission rates. Although the overall recurrence rate (21%, seven of 33 evaluated) was not different from previously published long-term studies, in three of seven cases of recurrence, early recurrences were noted between 2 and 4 months after remission. In patients who did not achieve remission, the most common and effective treatment options were repeat TSS,
-knife radiosurgery, and bilateral adrenalectomy.
Conclusion: The lower remission rate in patients without histological evidence of an adenoma is most likely a result of a decreased rate of adenoma extirpation. The incidence of early recurrence may be a unique feature of this patient population; patients without histological confirmation of tumor resection therefore require close and consistent monitoring postoperatively.
This article has been cited by other articles:
![]() |
C. G. Patil, D. M. Prevedello, S. P. Lad, M. L. Vance, M. O. Thorner, L. Katznelson, and E. R. Laws Jr. Late Recurrences of Cushing's Disease after Initial Successful Transsphenoidal Surgery J. Clin. Endocrinol. Metab., February 1, 2008; 93(2): 358 - 362. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Endocrinology | Endocrine Reviews | J. Clin. End. & Metab. |
| Molecular Endocrinology | Recent Prog. Horm. Res. | All Endocrine Journals |