Category LITFL
Rendu-Osler-Weber disease

Rendu-Osler-Weber disease

Rendu-Osler-Weber disease (aka Hereditary haemorrhagic telangiectasia (HHT)) is an autosomal dominant disorder characterised by epistaxis, cutaneous telangiectasia, and visceral arteriovenous malformations (AVMs).

May–Thurner syndrome

May–Thurner syndrome (MTS). Venous compression syndrome causing left-sided iliofemoral DVT, first anatomically defined by May and Thurner in 1957.

Josef Thurner

Josef Thurner (b. 1927), Austrian pathologist and co-eponym of May–Thurner syndrome; led pathology in Salzburg and published widely on venous disease.

Robert May

Robert May (1912–1984), pioneer of scientific phlebology; co-described May–Thurner syndrome and the May perforating vein, advancing venous diagnostics.

eponymictionary-340-256 2

Dercum’s disease

Overview of Dercum's disease: rare painful adipose‑tissue disorder, epidemiology, treatment strategies, and eponym history.

eponymythology atraumatic abdominal ecchymosis 340

Non-traumatic Abdominal Ecchymosis

Non-traumatic abdominal ecchymosis of the abdominal wall and flanks (Grey Turner, Cullen and Stabler); scrotum (Bryant) and upper thigh (Fox) as clues to potentially serious causes of abdominal pathology.

William Allen Sturge (1850-1919) 680

William Sturge

William Allen Sturge (1850–1919) English neurologist and archaeologist; first described Sturge-Weber syndrome; awarded MVO; pioneer of women’s medical education; noted collector of prehistoric artefacts.

Horner Syndrome 680

Horner Syndrome

Horner syndrome is associated with an interruption to the sympathetic nerve supply of the eye. It is characterized by the classic triad of miosis, partial ptosis, and anhidrosis +/- enophthalmos

Caleb Hillier Parry (1755-1822) 680

Caleb Hillier Parry

Caleb Hillier Parry 1755–1822 English physician described Hemifacial atrophy; angina pectoris; Hirschprung disease; Graves disease in 1825