EBV-Positive T-Cell Lymphoproliferative Disorder of Childhood
eosinophil disorder +
eosinophil peroxidase deficiency
functional neutrophil defect +
hereditary neutrophilia
human granulocytic anaplasmosis
Lambert-Eaton myasthenic syndrome
Langerhans Cell Histiocytosis
leukostasis
lymphopenia +
Mastocytosis +
neuralgic amyotrophy
neutropenia +
Opsoclonus-Myoclonus Syndrome
paraneoplastic cerebellar degeneration
paraneoplastic polyneuropathy
phagocyte bactericidal dysfunction +
POEMS syndrome
A multisystemic disorder characterized by a sensorimotor polyneuropathy (POLYNEUROPATHIES), organomegaly, endocrinopathy, monoclonal gammopathy, and pigmentary skin changes. Other clinical features which may be present include EDEMA; CACHEXIA; microangiopathic glomerulopathy; pulmonary hypertension (HYPERTENSION, PULMONARY); cutaneous necrosis; THROMBOCYTOSIS; and POLYCYTHEMIA. This disorder is frequently associated with osteosclerotic myeloma. (From Adams et al., Principles of Neurology, 6th ed, p1335; Rev Med Interne 1997;18(7):553-62) POEMS syndrome is a paraneoplastic syndrome characterized by polyradiculoneuropathy (P), organomegaly (O), endocrinopathy (E), clonal plasma cell disorder (M), and skin changes (S). Other features include papilledema, extravascular volume overload, sclerotic bone lesions, thrombocytosis/erythrocytosis, and elevated VEGF levels.
radiation-induced plexopathy
Small Intestinal Enteropathy-Associated T-Cell Lymphoma