Page 905 - Small Animal Internal Medicine, 6th Edition
P. 905

CHAPTER 50   Disorders of the Adrenal Gland   877


            hyperadrenocorticism, and prolonged survival with a good   less commonly, permanent central diabetes insipidus (CDI),
            quality of life. All studies evaluating the effect of irradiation   hypernatremia, keratoconjunctivitis sicca (KCS), and sec-
  VetBooks.ir  on pituitary tumor size, to date, have documented a signifi-  ondary hypothyroidism (Hanson et al., 2005). Postoperative
                                                                 hormonal replacement therapy included synthetic vasopres-
            cant decrease in tumor size in almost all dogs treated.
              Prognostic factors that affect survival time after radiation
                                                                 present until death or until latest follow-up in 22% of the dogs.
            therapy include the severity of neurologic signs and the rela-  sin (DDAVP), glucocorticoids, and levothyroxine. CDI was
            tive size of the tumor. Generally, dogs with subtle or mild   In another study, the incidence of postoperative permanent
            neurologic clinical signs and the smallest tumors show the   CDI in dogs undergoing transsphenoidal surgery for PDH
            best response to treatment. Theon et al. (1998) found a mean   was strongly influenced by the size of the pituitary tumor;
            survival time after radiation of 25 months in dogs with mild   the larger the tumor, the more likely for postoperative CDI to
            neurologic signs, 17 months in dogs with severe neurologic   be permanent (Teshima et al., 2011). Twelve of the 150 dogs
            signs, and only 5 months in untreated dogs with neurologic   died within 4 weeks of surgery. One-hundred twenty-seven
            signs. In a study by Kent et al. (2007), mean survival time in   (92%) of 138 dogs that were alive after 4 weeks experienced
            19 dogs with pituitary masses treated with radiation therapy   remission within 8 weeks of surgery; remission was defined
            was 1405 days, and 1-, 2-, and 3-year estimated survival was   as resolution of clinical signs of hyperadrenocorticism and
            93%, 87%, and 55%, respectively. In contrast, mean survival   UCCR values in the reference range. Hyperadrenocorticism
            time in 27 untreated dogs with pituitary masses was 551   remained in remission in 95 of 127 dogs (75%). In 32 of 127
            days, and 1-, 2-, and 3-year estimated survival was 45%, 32%,   dogs (25%), signs of hyperadrenocorticism and increased
            and 25%, respectively.                               UCCR values recurred at 6 weeks to 56 months (median, 18
              Because of the high prevalence of a pituitary mass at the   months) after surgery. The 1-year, 2-year, 3-year, and 4-year
            time PDH is diagnosed and the potential for future growth   estimated survival rate was approximately 84%, 76%, 72%,
            and development of neurologic signs, we routinely discuss   and 68%, respectively. The 1-year, 2-year, 3-year, and 4-year
            CT imaging of the pituitary gland as part of the evaluation   estimated relapse-free fraction was approximately 88%, 75%,
            of a dog with newly diagnosed PDH even if there is no clini-  66%, and 59%, respectively. Survival and disease-free frac-
            cal evidence of a large pituitary mass, especially if the client   tions of dogs with enlarged pituitaries were significantly
            is willing to consider irradiation therapy if a large pituitary   lower than in dogs with nonenlarged pituitaries.
            mass is identified. Our preference is to perform CT imaging   Based on the experiences at Utrecht University, micro-
            once clinical signs of hyperadrenocorticism are controlled   surgical transsphenoidal hypophysectomy is an effective
            with medical treatment. We understand that CT imaging is   long-term treatment of PDH in dogs. Early diagnosis of
            expensive but many of our clients are interested and want to   a  corticotroph  adenoma  is  important.  Transsphenoidal
            know the status of the pituitary mass. No further evaluation   hypophysectomy is most effective in dogs with nonenlarged
            of the pituitary is indicated if a pituitary mass is not identi-  or moderately enlarged pituitaries. Size of the pituitary
            fied on the initial CT scan. If a pituitary mass is identified   tumor has a direct impact on survival, disease-free fractions,
            and measures 3 to 7 mm in greatest vertical height, a repeat   and incidence of permanent CDI in dogs. Unfortunately,
            pituitary scan is recommended 12 months later. If a pituitary   the number of sites currently offering hypophysectomy as
            mass is identified equal to or greater than 8 mm in greatest   a treatment option for PDH is limited in the United States.
            vertical height, pituitary irradiation is recommended. The
            goal of pituitary irradiation is to shrink the mass and prevent   Prognosis
            development of macrotumor syndrome; trilostane or mito-  Reported median survival times for dogs with ADH that
            tane therapy may still be needed to control clinical signs of   survive the initial postadrenalectomy month range from 492
            hyperadrenocorticism.                                to 953 days, with some dogs living 4 to 5 years after surgery
                                                                 (Schwartz et al., 2008; Lang et al., 2011; Massari et al., 2011).
            HYPOPHYSECTOMY                                       In one study by Helm et al. (2011), median survival times
            For several decades, selective pituitary microsurgery using   for dogs with ADH treated with trilostane and mitotane were
            the transsphenoidal approach has been considered the treat-  353 days (95% confidence interval [CI], 95-528 days) and
            ment of choice for pituitary tumors causing hyperadreno-  102 days (95% CI, 43-277 days), respectively. Dogs with
            corticism in humans. Initial studies in veterinary medicine   adrenocortical adenoma or adrenocortical carcinoma that
            developing the microsurgical technique, identifying postop-  has not metastasized (uncommon) have a good prognosis,
            erative complications and assessing postoperative pituitary   whereas dogs with metastatic adrenocortical carcinoma or
            function, or lack thereof, were done in healthy dogs approxi-  carcinoma with vein invasion (common) have a poorer prog-
            mately 25 years ago. Since then, Meij and co-investigators at   nosis, and these dogs typically succumb to the disease within
            Utrecht University, the Netherlands, have published several   1 to 2 years of diagnosis. Although clinical signs can be
            articles detailing their experiences with transsphenoidal   controlled with trilostane and mitotane, death ultimately
            hypophysectomy in dogs with PDH. In 2005, the Utrecht   results from the debilitating effects of the tumor, complica-
            group reported on the long-term results of transsphenoidal   tions of vein thrombosis (e.g., ascites) or metastatic growth,
            hypophysectomy in 150 dogs with PDH (Hanson et al.,   or  other  geriatric  disorders  (e.g.,  chronic  kidney  disease,
            2005). Postoperative complications included transient and,   congestive heart failure).
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