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2.
Acta Otolaryngol ; 129(5): 545-9, 2009 May.
Article in English | MEDLINE | ID: mdl-18720067

ABSTRACT

CONCLUSIONS: CT of the sinuses showed long-lasting improvement in the total and CT scores of the osteomeatal complex (OMC) after combined surgical and corticosteroid treatment as compared with medical treatment alone. However, the correlations between the improved CT scores and the patients' symptoms, olfactory thresholds or polyp scores were generally not significant. OBJECTIVE: To evaluate CT scans as a method for comparing the effect of medical treatment versus combined surgical and medical treatment of nasal polyposis. PATIENTS AND METHODS: Thirty-two patients with nasal polyposis were randomized to unilateral endoscopic sinus surgery after pretreatment with oral prednisolone for 10 days and nasal budesonide bilaterally for 1 month. Postoperatively, they were given nasal steroids (budesonide) bilaterally for 1 year. They were assessed with nasal endoscopy, symptom scores, and olfactory thresholds and followed for 12 months. CT of the sinuses was performed before and 1 year after operation. The CT scans were evaluated using the Lund staging system. RESULTS: From before surgery to 1 year after surgery, we found a significant improvement on the operated side in the CT total scores, and scores of the OMC and the maxillary sinus, but no significant differences on the unoperated side. Significant correlations were also noted between the differences in olfactory thresholds between the operated and unoperated sides.


Subject(s)
Nasal Polyps/diagnostic imaging , Nasal Polyps/therapy , Adrenal Cortex Hormones/therapeutic use , Adult , Endoscopy , Female , Humans , Male , Middle Aged , Nasal Polyps/surgery , Postoperative Care , Preoperative Care , Prospective Studies , Surgery, Computer-Assisted , Tomography, X-Ray Computed , Treatment Outcome , Young Adult
4.
J Neurosurg ; 100(4): 634-8, 2004 Apr.
Article in English | MEDLINE | ID: mdl-15070117

ABSTRACT

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.


Subject(s)
Adenoma/complications , Adenoma/surgery , Cushing Syndrome/surgery , Neurosurgical Procedures/methods , Pituitary Neoplasms/complications , Pituitary Neoplasms/surgery , Radiosurgery/methods , Adolescent , Adult , Aged , Female , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Recurrence , Retrospective Studies , Sphenoid Bone/surgery , Treatment Outcome
5.
Regul Pept ; 117(2): 127-39, 2004 Feb 15.
Article in English | MEDLINE | ID: mdl-14700749

ABSTRACT

Tumor galanin content was measured in extracts from human pituitary adenomas using a specific RIA method for monitoring human galanin. Twenty-two out of twenty-four tumors contained galanin with notably high levels in corticotroph adenomas, varying levels in clinically inactive tumors, and low levels in GH secreting adenomas. Tumor galanin and ACTH contents were closely correlated in all tumors. In four young patients with microadenomas and highly active Mb Cushing tumor galanin was inversely related to tumor volume. The molecular form of tumor galanin, studied with reverse-phase HPLC, was homogeneous with the majority of tumor galanin coeluting with standard human galanin. In the tumors analysed with in situ hybridization there was a good correlation between galanin peptide levels and galanin mRNA expression. In some tumors galanin mRNA and POMC levels coexisted, in others they were essentially in different cell populations. Levels of plasma galanin-LI were not related to tumor galanin concentration, and galanin levels were in the same range in sinus petrosus close to the pituitary venous drainage as in peripheral blood. Corticotrophin releasing hormone injections in two patients caused ACTH, but no detectable galanin release into sinus petrosus. Our results demonstrate that corticotroph, but not GH adenomas, express high levels of galanin, in addition to ACTH, and that in some tumors both polypeptides are synthesised in the same cell population. However, galanin levels in plasma were not influenced by the tumor galanin content.


Subject(s)
Adenoma/metabolism , Galanin/metabolism , Pituitary Neoplasms/metabolism , Adrenocorticotropic Hormone/blood , Adult , Aged , Chromatography, High Pressure Liquid , Female , Humans , In Situ Hybridization, Fluorescence , Male , Middle Aged , Oligonucleotide Probes , Radioimmunoassay
6.
Acta Otolaryngol ; 123(7): 862-8, 2003 Sep.
Article in English | MEDLINE | ID: mdl-14575403

ABSTRACT

OBJECTIVE: To compare the effect on olfaction of topical glucocorticoid treatment versus placebo given for an extended period in addition to oral short-term glucocorticoids in patients with anosmia/hyposmia. MATERIAL AND METHODS: This was a randomized, double-blind, placebo-controlled study. The criterion for inclusion in the blinded phase was an improvement of at least 2 steps in the butanol odor threshold test following open treatment for 10 days with oral and nasal corticosteroids. Forty patients were included: 20 were randomized to treatment with fluticasone propionate, 10 to placebo and 10 others as controls. The topical treatment was continued for 6 months. RESULTS: The 3 groups showed similar improvements in their sense of smell after the initial 10-day treatment with combined oral and nasal corticosteroids. Patients who continued the local treatment maintained the same level of improvement throughout the study, whether or not they had been given nasal corticosteroids or placebo. We found no significant differences between the treatment groups. CONCLUSIONS: In patients with anosmia/hyposmia partly caused by local inflammation, no further improvement in the olfactory threshold is achieved by continuing with a topical intranasal glucocorticoid after an initial combined topical and systemic glucocorticoid treatment.


Subject(s)
Androstadienes/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Olfaction Disorders/drug therapy , Smell/drug effects , Administration, Topical , Adolescent , Adult , Androstadienes/pharmacology , Anti-Inflammatory Agents/pharmacology , Double-Blind Method , Female , Fluticasone , Humans , Male , Middle Aged , Olfaction Disorders/physiopathology , Tomography, X-Ray Computed , Treatment Outcome
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