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Transsphenoidal surgery in Cushing disease : 10 years of experience in 34 consecutive cases

Höybye, Charlotte (författare)
Karolinska Institutet
Grenbäck, Eva (författare)
Departments of Endocrinology and Diabetology, Otorhinolaryngology and Head and Neck Surgery, and Neurosurgery, Karolinska Hospital, Stockholm
Thorén, Marja (författare)
Karolinska Institutet
visa fler...
Hulting, Anna-Lena (författare)
Karolinska Institutet
Lundblad, Lars (författare)
Departments of Endocrinology and Diabetology, Otorhinolaryngology and Head and Neck Surgery, and Neurosurgery, Karolinska Hospital, Stockholm
Änggård, Anders (författare)
von Holst, Hans (författare)
Karolinska Institutet
visa färre...
 (creator_code:org_t)
Journal of Neurosurgery Publishing Group (JNSPG), 2004
2004
Engelska.
Ingår i: Journal of Neurosurgery. - : Journal of Neurosurgery Publishing Group (JNSPG). - 0022-3085 .- 1933-0693. ; 100, s. 634-638
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Object. Cushing disease is a rare disorder. Because of their small size the adrenocorticotropic hormone (ACTH)—producing tumors are often not detectable on neuroimaging studies. To obtain a cure with transsphenoidal surgery (TSS) may therefore be difficult. In this report the authors present 10 years of experience in the treatment of patients with Cushing disease who were followed up with the same protocol and treated by the same surgeon.Methods. Thirty-four patients, 26 of them female and eight of them male (mean age 40 years, range 13–74 years) were studied. All had obvious clinical signs and symptoms of Cushing syndrome. Magnetic resonance (MR) imaging was performed in all patients, and inferior petrosal sinus (IPS) sampling was done in 14.In 12 patients MR imaging indicated a pituitary tumor; 10 were microadenomas and two were macroadenomas. In six patients with no visible tumor, the results of IPS sampling supported the diagnosis. All patients underwent TSS; the mean follow-up duration was 6 ± 0.5 years. Selective adenomectomy was performed in 32 and hemihypophysectomy in the other two patients. A cure was obtained in 31 patients (91%) after one TSS and in two more patients after further TSS; one patient was not cured despite two TSSs and one underwent bilateral adrenalectomy. Disease recurrence was seen in two patients after 3 years, and they were successfully treated with stereotactic gamma knife surgery. Half of the patients had an ACTH deficiency postoperatively, whereas one third had other pituitary hormone insufficiencies. There were no serious complications attributable to the surgical intervention.Conclusions. Transsphenoidal surgery with selective adenomectomy is an effective and safe treatment for Cushing disease. In the patients presented in this study, the surgical outcome seemed to depend on careful preoperative evaluation and the surgeon's experience. For optimal results in this rare disease the authors therefore suggest that the endocrinological, radiological, and surgical procedures be coordinated in a specialized center.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kirurgi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Surgery (hsv//eng)

Nyckelord

Cushing disease
transsphenoidal surgery
outcome

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