Searchable abstracts of presentations at key conferences in endocrinology

ea0035p670 | Growth hormone IGF axis basic | ECE2014

Young female with acromegaloid features, pituitary macroadenoma, and an uncomplicated pregnancy

Figueroa Carlos , Santiago Monica , Hernan Jose , Mangual Michelle , Gutierrez Madeleine , Palermo Coromoto , Trinidad Rafael , Sanchez Alfredo , Miranda Maria DeLourdes

Thirty-two years old female G2P1A0 seen at our endocrinology clinic 9 years ago complaining of persistent menstrual irregularities associated to elevated prolactin values. MRI done revealed a pituitary microadenoma. However, she refused treatment for microprolactinoma. Four years afterwards, patient return complaining of recurrent episodes of headache. Repeated MRI showed a pituitary macroadenoma, so start on cabergoline treatment.Once more, patient was ...

ea0032p1132 | Thyroid cancer | ECE2013

Male patient with neck mass: ectopic cancer vs metastasic disease

Palermo Coromoto , Torres Oberto , Hernan Martinez Jose , Silva Frieda , Gutierrez Madeleine , Gonzalez Eva , de Lourdes Miranda Maria

Case of 33 years old male patient with an unremarkable past medical history, who after a car accident, a cystic nodular right neck mass was incidentally found by MRI of cervical spine. Physical examination revealed a mildly tender right neck mass. He was clinically and biochemically euthyroid. Denied history of neck irradiation. No family history of thyroid disease or thyroid cancer. Excisional biopsy of right neck mass showed metastasic well differentiated papillary carcinoma...

ea0035p257 | Clinical case reports Pituitary/Adrenal | ECE2014

Acromegaly with a normal pituitary gland

Cruz Alfredo Sanchez , Martinez Jose H , de Lourdes Miranda Maria , Palermo Coromoto , Gonzalez Eva , Torres Oberto , Santiago Monica , Figueroa Carlos , Trinidad Rafael , Mangual Michelle , Gutierrez Madeleine

Background: Acromegaly most commonly results from an excess production of GH and secondary increase in IGF1. More than 95% of the time from the pituitary gland, but the source of excess GH secretion may not necessarily be pituitary in origin. Ectopic acromegaly may arise due to neuroendocrine tumors by production of GHRH and in <0.5% of the cases from ectopic pituitary remnants in the sphenoid sinus.Clinical case: We present a case of a 37 years old ...

ea0035p866 | Pituitary Clinical (<emphasis role="italic">Generously supported by IPSEN</emphasis>) | ECE2014

A middle aged woman with isolated ACTH deficiency associated with transient GH deficiency

Mangual Michelle , Hernan-Martinez Jose , Santiago Monica , Figueroa Carlos , Trinidad Rafael , Gutierrez Madeleine , Sanchez Alfredo , Palermo Coromoto , Miranda Maria De Lourdes , Torres Oberto , Gonzalez Eva

Introduction: Isolated ACTH deficiency (IAD) is a rare entity characterized by secondary adrenal insufficiency with low levels of serum cortisol, decreased production of ACTH, adequate secretion of other pituitary hormones and normal pituitary structure on radioimaging. Due to the rarity of its occurrence the prevalence of IAD as a cause of secondary adrenal insufficiency has not been determined. To our knowledge 200 cases are described in the literature. Impairment of GH secr...

ea0035p990 | Thyroid (non-cancer) | ECE2014

The prevalence of coexistence thyroid carcinoma and thyroid nodules in hyperthyroid patients of San Juan City Hospital

Santiago Monica , Hernan-Martinez Jose , Palermo Coromoto , Figueroa Carlos , Trinidad Rafael , Mangual Michelle , Gutierrez Madeleine , De Lourdes Miranda Maria , Gonzalez Eva

Hyperfunctional nodules of the thyroid are rarely associated with thyroid cancer, for these reason are rarely biopsied. Although multiple theories have being proposed, the relationship is still uncertain. After performing a MEDLINE literature search, we found in multiple retrospectives analysis, that patients with hyperthyroidism with hyperfunctional nodules have an estimated of 0.3–16.3% prevalence of malignancy. In our study forty-eight hyperthyroid cases were prospecti...