A case of Lemierre’s syndrome causing panhypopituitarism, cavernous sinus thrombosis, ischaemic stroke and pulmonary embolism

Author:

Dewdney Charlotte J1,Anderson Joseph J2,Dewar Simon2,Doubal Fergus3,Burgess Frederick R4,Subedi Deepak5,Lyall Marcus J1

Affiliation:

1. Edinburgh Centre for Endocrinology and Diabetes, NHS Lothian, Edinburgh, UK

2. Department of Medical Microbiology, NHS Lothian, Edinburgh, UK

3. Centre for Clinical Brain Sciences, Edinburgh Neuroscience, Edinburgh, UK

4. Department of Ophthalmology, Princess Alexandra Eye Pavilion, Edinburgh, UK

5. Department of Radiology, Royal Infirmary of Edinburgh, NHS Lothian, Edinburgh, UK

Abstract

Infection is a rare cause of panhypopituitarism and has not been reported in the context of Lemierre’s syndrome. We present the case of a previously well 19-year-old man, who presented acutely unwell with meningitis and sepsis. Fusobacterium necrophorum was isolated from peripheral blood cultures and identified on cerebrospinal fluid with 16S rDNA Polymerase Chain Reaction (PCR). Imaging demonstrated internal jugular vein thrombosis with subsequent cavernous venous sinus thrombosis. Pituitary function tests were suggestive of panhypopituitarism. The patient was diagnosed with Lemierre’s syndrome complicated by meningitis, cavernous sinus thrombosis, base of skull osteomyelitis, ischaemic stroke and panhypopituitarism. He was treated with 13 weeks of intravenous antibiotics followed by 3 weeks of oral amoxicillin, and anticoagulated with dalteparin then apixaban. His panhypopituitarism was managed with hydrocortisone, levothyroxine and desmopressin.

Publisher

SAGE Publications

Subject

Education,General Medicine

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