Granulocytosis: Difference between revisions

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===In alphabetical order===
*[[Acute intermittent porphyria]]
*[[Acute myeloid leukemia]]
*[[Acute pancreatitis]]
*[[Acute promyelocytic leukemia]]
*[[Still's disease|Adult-onset Still's disease]]
*[[Aminophylline]]
*[[Bronchiolitis obliterans organizing pneumonia]]
*[[Chronic myeloid leukaemia]]
*[[Congenital syphilis]]
*[[Dinoprostone]]
*[[Extrinsic allergic alveolitis]]
*[[Filgrastim]]
*[[Gallbladder empyema]]
*[[Granulocyte colony stimulating factor]]
*[[Granulocyte-macrophage colony stimulating factor]]
*[[Hantavirus]]
*[[Hereditary neutrophilia]]
*[[Hyperimmunoglobulinemia D and periodic fever syndrome]]
*[[Leukocyte adhesion deficiency|Leukocyte adhesion deficiency type 1]]
*[[Leukocyte adhesion deficiency|Leukocyte adhesion deficiency type 2]]
*[[Leukocyte adhesion deficiency|Leukocyte adhesion deficiency type 3]]
*[[Leukemoid reaction]]
*[[Lithium]]
*[[Lymphangitis]]
*[[Mast cell leukemia]]
*[[Polycythaemia rubra vera]]
*[[Recurrent hereditary polyserositis]]
*[[ARDS|Severe acute respiratory syndrome]]
*[[Splenectomy]]
*[[Sulprostone]]
*[[Uric acid|Urate crystal]] [[arthropathy]]
*[[Wegener granulomatosis]]


==Related Chapters==
==Related Chapters==

Revision as of 17:20, 25 April 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-In-Chief: Lakshmi Gopalakrishnan, M.B.B.S. [2]

Overview

  • Granulocytosis can be a feature of a number of diseases:

Differential Diagnosis of Causes of Granulocytosis

By Organ System

Cardiovascular No underlying causes
Chemical / poisoning No underlying causes
Dermatologic No underlying causes
Drug Side Effect Aminophylline, Dinoprostone, Filgrastim, Granulocyte colony stimulating factor, Granulocyte-macrophage colony stimulating factor, Lithium, Sulprostone
Ear Nose Throat No underlying causes
Endocrine No underlying causes
Environmental No underlying causes
Gastroenterologic Acute pancreatitis, Gallbladder empyema
Genetic Acute intermittent porphyria, Hereditary neutrophilia, Hyperimmunoglobulinemia D and periodic fever syndrome, Leukocyte adhesion deficiency type 1, Leukocyte adhesion deficiency type 2, Leukocyte adhesion deficiency type 3, Recurrent hereditary polyserositis
Hematologic Acute intermittent porphyria, Leukemoid reaction, Leukocyte adhesion deficiency type 1, Leukocyte adhesion deficiency type 2, Leukocyte adhesion deficiency type 3, Lymphangitis, Polycythaemia rubra vera, Recurrent hereditary polyserositis
Iatrogenic Splenectomy
Infectious Disease Congenital syphilis, Hantavirus
Musculoskeletal / Ortho No underlying causes
Neurologic No underlying causes
Nutritional / Metabolic No underlying causes
Obstetric/Gynecologic No underlying causes
Oncologic Acute myeloid leukemia, Acute promyelocytic leukemia, Chronic myeloid leukaemia, Mast cell leukemia, Polycythaemia rubra vera
Opthalmologic No underlying causes
Overdose / Toxicity No underlying causes
Psychiatric No underlying causes
Pulmonary Bronchiolitis obliterans organizing pneumonia, Extrinsic allergic alveolitis, Wegener granulomatosis, Severe acute respiratory syndrome
Renal / Electrolyte Wegener granulomatosis
Rheum / Immune / Allergy Adult-onset Still disease, Urate crystal arthropathy, Wegener granulomatosis
Sexual No underlying causes
Trauma No underlying causes
Urologic No underlying causes
Miscellaneous No underlying causes

In alphabetical order

Related Chapters

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