Graves’ ophthalmopathy occurs in 25% – 50% of patients with Graves’ Hyperthyroidism. Euthyroid Graves’ ophthalmopathy is much less common, occurring in approximately 10% of patients with Graves’ ophthalmopathy (1). Review of the literature revealed no reports of euthyroid Graves’ ophthalmopathy in children. The case of an eight-year old female with euthyroid Graves’ ophthalmopathy is reported.
This manuscript has been assigned to a volume and issue but has not yet been published. It is either being edited, typeset or is in the proof stage of publication.
In the pre-published stage, this manuscript may contain statements, opinions, and information that have errors in facts, figures, or interpretation. Any final changes in this manuscript will be made at the time of publication and will be reflected in the final electronic version of the issue. The editors and authors and their respective employees are not responsible or liable for the use of any such inaccurate or misleading data, opinion or information contained in the articles in this section.
This is a report of a case with both peritoneal tuberculosis and gastric cancer. Physicians should have a high index of suspicion of peritoneal tuberculosis if the patient is febrile with a past history of tuberculosis.
Tracheobronchial stenting via flexible bronchoscopy has been performed at the National Chest Hospital, Kingston, Jamaica, for just over a year. Whereas stents have been used in the management of tracheo-oesophageal fistulae, this is the first case of a tracheobronchial stent being deployed for management of a bronchopleural fistula at this institution.
A 32-year old male, with a history of depression and previous suicide attempts, was brought to hospital comatose after ingestion of brake fluid. He developed severe metabolic acidosis with an increased anion gap, hypotension, seizures and mild renal impairment. He required intensive care treatment for ventilatory and inotropic support. The clinical features, diagnosis and treatment of this unusual poison are discussed.
Patients with Russell-Silver Syndrome are a challenge to the anaesthetist because of the variety of anomalies. Appropriate anaesthetic and surgical management can lead to uneventful experiences with these patients.
Polyarteritis nodosa with gallbladder involvement is a rare condition. Autosomal dominant polycystic kidney disease is also a rare condition and rarely complicated. We describe an extremely rare case of Polyarteritis nodosa, involving gallblader and ureter without obstruction, in a patient with autosomal dominant polycystic kidney disease. To the best of the authors’ knowledge, such a case has not been reported previously.