Multiple myeloma (MM) is a plasmocytic malignant proliferation of a single clone resulting in an overabundance of monoclonal immunoglobulins. MM commonly presents with bone disorders, renal failure, anaemia and hypercalcaemia. Hyperviscosity syndrome is rare, as are vaso-occlusive symptoms. The authors report a dramatic case of an 80-year-old woman admitted to the emergency department with full-blown distal gangrene. The culprit turned out to be a MM, unusually presenting with symptomatic hyperviscosity and peripheral occlusive ischaemia. This catastrophic and particularly dramatic presentation is almost unprecedented, with only a few cases reported worldwide
Objectives: Infectious agents triggering haemophagocytic lymphohistiocytosis (HLH) primarily involve...
A review essay of Hans Lindahl, Fault Lines of Globalization (OUP, 2013).Peer reviewe
This paper reports on research in progress that explores the potential role the materiality of thing...
Syphilis is a sexually transmitted disease known to present with highly variable manifestations, esp...
Objectives: We report a case of primary melanoma of the small intestine. Primary intestinal melanoma...
Autoimmune diseases may present as paraneoplastic syndrome. This is especially recognized in the cas...
A 76-year-old man was admitted to hospital with fever, weight loss, pancytopenia, hepatosplenomegaly...
Crohn’s disease is a granulomatous inflammatory bowel disease. Its pathologic findings include non-con...
Introduction: Auricular chondritis has been occasionally described in patients with systemic lupus e...
Richard Corlett looks at the stereotype of the ‘Essex girl’ beyond its portrayal in the media
Objectives: Thrombocytopenia and splenomegaly are common features in several haematological disorder...
Immune-mediated necrotizing myopathies (IMNM) are recognized as a subgroup of idiopathic inflammator...
In dit proefschrift wordt de klinische betekenis onderzocht van atherosclerotisch nier arterie steno...
Hereditary angioedema (HAE) is a rare genetic disorder transmitted as an autosomal dominant trait, c...
We present a rare case of a 23-year-old male incidentally detected with hepatitis B virus (HBV) infe...
Objectives: Infectious agents triggering haemophagocytic lymphohistiocytosis (HLH) primarily involve...
A review essay of Hans Lindahl, Fault Lines of Globalization (OUP, 2013).Peer reviewe
This paper reports on research in progress that explores the potential role the materiality of thing...
Syphilis is a sexually transmitted disease known to present with highly variable manifestations, esp...
Objectives: We report a case of primary melanoma of the small intestine. Primary intestinal melanoma...
Autoimmune diseases may present as paraneoplastic syndrome. This is especially recognized in the cas...
A 76-year-old man was admitted to hospital with fever, weight loss, pancytopenia, hepatosplenomegaly...
Crohn’s disease is a granulomatous inflammatory bowel disease. Its pathologic findings include non-con...
Introduction: Auricular chondritis has been occasionally described in patients with systemic lupus e...
Richard Corlett looks at the stereotype of the ‘Essex girl’ beyond its portrayal in the media
Objectives: Thrombocytopenia and splenomegaly are common features in several haematological disorder...
Immune-mediated necrotizing myopathies (IMNM) are recognized as a subgroup of idiopathic inflammator...
In dit proefschrift wordt de klinische betekenis onderzocht van atherosclerotisch nier arterie steno...
Hereditary angioedema (HAE) is a rare genetic disorder transmitted as an autosomal dominant trait, c...
We present a rare case of a 23-year-old male incidentally detected with hepatitis B virus (HBV) infe...
Objectives: Infectious agents triggering haemophagocytic lymphohistiocytosis (HLH) primarily involve...
A review essay of Hans Lindahl, Fault Lines of Globalization (OUP, 2013).Peer reviewe
This paper reports on research in progress that explores the potential role the materiality of thing...