Page 919 - Small Animal Internal Medicine, 6th Edition
P. 919

CHAPTER 50   Disorders of the Adrenal Gland   891



                   TABLE 50.6
  VetBooks.ir  Adrenal Tumors Reported in Dogs and Cats                              TESTS TO ESTABLISH


                              HORMONE SECRETED      SPECIES    CLINICAL SYNDROME     DIAGNOSIS

             Nonfunctional    None                  Dog,* Cat  —                     Diagnosis by exclusion
               adrenal tumor                                                           histopathology
             Functional       Cortisol              Dog,* Cat  Hyperadrenocorticism   Urine C:C ratio
               adrenocortical                                    Cushing’s syndrome  Low-dose dexamethasone
               tumor                                                                   suppression test
                                                                                            +
                              Aldosterone           Cat,* Dog  Hyperaldosteronism    Serum K  and Na +
                                                                 Conn’s syndrome     Baseline plasma aldosterone
                              Progesterone          Cat,* Dog  Mimics                Serum progesterone
                                                                 hyperadrenocorticism
                              Steroid hormone precursors
                                17-OH-progesterone  Dog, Cat   Mimics                ACTH stimulation test—
                                                                 hyperadrenocorticism  measures steroid hormone
                                                                                       precursors
                                Desoxycorticosterone  Dog      Mimics                ACTH stimulation test—measures
                                                                 hyperaldosteronism    steroid hormone precursors
             Functional       Norepinephrine        Dog,* Cat  Pheochromocytoma      Urine normetanephrine to
               adrenomedullary   Epinephrine                                           creatinine ratio; Plasma free
               tumor                                                                   normetanephrine concentration
            ACTH, Adrenocorticotropic hormone.
            *Species most commonly affected.



            relies on histologic evaluation of the surgically excised     protocol for the management of hypertension in dogs with
            adrenal mass.                                        pheochromocytoma  includes  preoperative  phenoxybenza-
                                                                 mine  and intraoperative  phentolamine.  The initial dosage
            Treatment                                            of phenoxybenzamine is 0.5 mg/kg q12h. Unfortunately,
            A period of medical therapy intended to reverse the effects   many dogs with pheochromocytoma have episodic clinical
            of excessive adrenergic stimulation, followed by surgical   signs and hypertension, making it difficult to adjust dosage
            removal of the tumor, is the treatment of choice for pheo-  on  the  basis  of  improvement  in  clinical  signs  and  blood
            chromocytoma. The success of chemotherapy and radiation   pressure. In addition, this dosage is often ineffective in pre-
            therapy in humans with pheochromocytoma has been     venting severe hypertension during surgery. Therefore we
            limited, and results of chemotherapy or radiation therapy for   gradually increase the phenoxybenzamine dosage every 3
            the treatment of pheochromocytoma in dogs or cats have not   to 4 days until clinical signs of hypotension (e.g., lethargy,
            been reported. Mitotane and trilostane are ineffective for   weakness, syncope), adverse drug reactions (e.g., vomiting),
            tumors arising from the adrenal medulla and are not recom-  or a maximum dosage of 2 mg/kg q12h is attained. Surgery
            mended. Long-term medical therapy is primarily designed   is recommended 1 to 2 weeks later either by laparotomy or
            to control excessive catecholamine secretion.        laparoscopic adrenalectomy. The drug should be continued
              Potentially life-threatening complications are common   until the time of surgery. Complications may occur despite
            during the perioperative period, especially during induc-  prior treatment with  α-adrenergic blocking drugs; close
            tion of anesthesia and manipulation of the tumor during   monitoring of the dog during the perioperative period is
            surgery. The most worrisome complications include episodes   critical for a successful outcome after adrenalectomy. (See
            of acute, severe hypertension (systolic arterial blood pressure   Suggested Readings for more information on the periopera-
            > 300 mm Hg), episodes of severe tachycardia (heart rate     tive and surgical management of dogs with a pheochromo-
            > 250 beats/min) and arrhythmias, and hemorrhage. Pre-  cytoma.) In a study by Herrera et al. (2008), the significant
            operative α-adrenergic blockade using phenoxybenzamine   prognostic indicators for survival after adrenalectomy for
            helps control potentially life-threatening fluctuations of blood   pheochromocytoma included lack of intraoperative arrhyth-
            pressure and heart rate during anesthesia and surgery. The   mias, decreased surgical time, younger age, and pretreat-
            dose  and  frequency  of  phenoxybenzamine  administration   ment with phenoxybenzamine.
            and the duration of therapy required to adequately achieve   Medical management with α-adrenergic blockade is rec-
            desired effects have not been defined for dogs. Our current   ommended whenever pheochromocytoma is suspected and
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