Cephalometric comparison between an acromegalic patient and his twin brother

Resumen: La acromegalia es una enfermedad caracterizada por una desfiguraci ón somática de progresión lenta causada por la sobreproducción de hormona de crecimiento (GH) y factor de crecimiento insulinoide tipo 1 (IGF-1), predominantemente asociada con un adenoma hipofisario. La manifestación más evidente a nivel facial es un prognatismo mandibular por exceso de creci miento de la mandíbula. El propósito del presente trabajo fue realizar una comparación morfológica craneofacial mediante análisis cefalométrico y superposición cefalométrica entre un paciente con diagnóstico de acromegalia y su hermano gemelo que no presenta la enfermedad. Nuestros resultad os mostraron que en el hermano con acromegalia existe un significativo aumento del tamaño de la silla turca, un desplazamiento hacia anterior del maxilar y mandíbula, siendo más marcado el desplazamiento mandibular. El cambio morfológico que experimenta la mandíbula en la acromegalia es atribui do principalmente al crecimiento de la rama mandibular por aumento de la unidad condilar.Abstract: Acromegaly is characterized by a slowly progressive somatic disfigurement caused by the overproduction of growth hormone (GH) and insulin-like growth factor 1 (IGF 1), mainly associated with a pituitary adenoma. The most evident facial manifestation is mandibular prognathism due to excessive growth of...
Source: Odontoestomatologia - Category: Dentistry Source Type: research

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Source: ClinicoEconomics and Outcomes Research - Category: Health Management Tags: ClinicoEconomics and Outcomes Research Source Type: research
AbstractObjectiveAlthough the focus of acromegaly treatment is the hormonal control of the disease, a new perspective must be given to the functional rehabilitation of these patients, especially when considering the recent increase in survival. The aim of this study was to evaluate the effects of therapist-oriented home rehabilitation (TOHR) on patients with acromegaly.Patients and methodsSeventeen adults with acromegaly followed an exercise programme from a booklet with instructions for each exercise prescribed, for 2 months, and were reassessed after 1 month of washout. At each of the 3 timepoints (before and after the i...
Source: Endocrine - Category: Endocrinology Source Type: research
This study used PLGA 5050 4H (F-1), PLGA 5050 1A: PLGA 5050 4H = 3:7 (F-2) and PLGA 7525 1A: PLGA 5050 4H = 3:7 (F-3) as a carrier, respectively. Microspheres (MS) were obtained by O/W emulsion solvent evaporation technique and characterized by scanning electron microscopy (SEM), particle size, drug loading, fluorescence characteristics, and in vitro and in vivo release. Accelerated tests in vitro showed that the size and number of core pores significantly affected drug release in the first and second phases. After intramuscular administration, F-2 and F-3 showed effective blood concentration levels and their bioav...
Source: European Journal of Pharmaceutical Sciences - Category: Drugs & Pharmacology Authors: Tags: Eur J Pharm Sci Source Type: research
CONCLUSION: These data demonstrate that high-dose Sandostatin LAR as monotherapy or in combination with pegvisomant or cabergoline is a feasible salvage option in patients with pituitary adenomas not adequately controlled on conventional SSA regimens. PMID: 31274183 [PubMed - as supplied by publisher]
Source: Endokrynologia Polska - Category: Endocrinology Authors: Tags: Endokrynol Pol Source Type: research
Pituitary adenomas are a rare but important central nervous system tumor in children. Because of differences in growth and development, the manifestations of pituitary adenomas in children may differ from those seen in adults. Unlike adult patients, the pediatric population more often presents with clinically secretory adenomas. Although medical management is first-line treatment of prolactinomas, transsphenoidal surgery is appropriate for most children with Cushing disease and gigantism. Although some pediatric patients present surgical challenges because of small anatomic dimensions or an incompletely developed sphenoid ...
Source: Neurosurgery Clinics of North America - Category: Neurosurgery Authors: Source Type: research
Condition:   Acromegaly Intervention:   Sponsor:   Ipsen Not yet recruiting
Source: ClinicalTrials.gov - Category: Research Source Type: clinical trials
Abstract Interdisciplinary Management of Sellar Masses Abstract. Sellar masses may present with an impairment of pituitary function (hypopituitarism), hormone hypersecretion (prolactinoma, acromegaly, glucocorticoid excess) or neurological symptoms (visual impairment, headache). An increasing number of them is discovered as an incidentaloma. Among the various entities, benign pituitary adenomas and cystic lesions are most frequently encountered. The work-up includes a laboratory evaluation for hormone hyper- or hyposecretion and an MRI of the pituitary gland. If the optic chiasm is compromised, a visual field exam...
Source: Praxis - Category: General Medicine Authors: Tags: Praxis (Bern 1994) Source Type: research
ConclusionsAlthough it rarely reveals CNC, acromegaly is diagnosed at a younger age in this setting, with a higher proportion of microadenomas.
Source: Pituitary - Category: Endocrinology Source Type: research
Conclusions: This radiomics model can assist neurosurgeons in predicting the tumor consistency in patients with acromegaly before surgery and facilitate the determination of individualized therapeutic schemes.
Source: Frontiers in Endocrinology - Category: Endocrinology Source Type: research
In this paper, the authors provide recommendations regarding the appropriate use of pasireotide long-acting release in the treatment of acromegaly.Journal of Clinical Endocrinology &Metabolism
Source: Medscape General Surgery Headlines - Category: Surgery Tags: Diabetes & Endocrinology Journal Article Source Type: news
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