1.A rare case of community acquired Burkholderia cepacia infection presenting as pyopneumothorax in an immunocompetent individual.
Suman S KARANTH ; Hariharan REGUNATH ; Kiran CHAWLA ; Mukhyaprana PRABHU
Asian Pacific Journal of Tropical Biomedicine 2012;2(2):166-168
Burkholderia cepacia (B. cepacia) infection is rarely reported in an immunocompetent host. It is a well known occurence in patients with cystic fibrosis and chronic granulomatous disease where it increases both morbidity and mortality. It has also been included in the list of organisms causing nosocomial infections in an immunocompetent host, most of them transmitted from the immunocompromised patient in which this organism harbors. We report a rare case of isolation of B. cepacia from the bronchoalveolar lavage fluid of an immunocompetent agriculturist who presented with productive cough and fever associated with a pyopneumothorax. This is the first case of community acquired infection reported in an immunocompetent person in India.
Adult
;
Anti-Bacterial Agents
;
therapeutic use
;
Azithromycin
;
therapeutic use
;
Bronchoalveolar Lavage Fluid
;
microbiology
;
Burkholderia Infections
;
diagnosis
;
drug therapy
;
transmission
;
Burkholderia cepacia
;
drug effects
;
isolation & purification
;
Ceftazidime
;
therapeutic use
;
Ceftizoxime
;
therapeutic use
;
Community-Acquired Infections
;
diagnosis
;
drug therapy
;
Drug Resistance, Multiple, Bacterial
;
Humans
;
Immunocompetence
;
India
;
Male
;
Pneumothorax
;
complications
2.Idiopathic intracranial hypertension, empty sella turcica and polycystic ovary syndrome--a case report.
K G Au EONG ; S HARIHARAN ; E C CHUA ; S LEONG ; M C WONG ; P S TSENG ; V S YONG
Singapore medical journal 1997;38(3):129-130
Permanent visual loss is a well established major sequela of idiopathic intracranial hypertension (IIH). It is often insidious and frequently unnoticed by patients with IIH. It is vital to monitor these patients with serial perimetric and visual acuity tests because visual loss can be halted and occasionally reversed if treatment is begun early. We report a case of IIH with an empty sella turcica and polycystic ovary syndrome who developed visual field loss over ten years. This report illustrates the importance of close ophthalmic monitoring and detailed neurological and endocrinological evaluation to prevent complications in such patients.
Adult
;
Chronic Disease
;
Empty Sella Syndrome
;
complications
;
diagnosis
;
Female
;
Humans
;
Polycystic Ovary Syndrome
;
complications
;
diagnosis
;
Pseudotumor Cerebri
;
complications
;
diagnosis
;
Vision Disorders
;
diagnosis
;
etiology