Granulomatosis with polyangiitis history and symptoms: Difference between revisions

Jump to navigation Jump to search
No edit summary
 
(24 intermediate revisions by 2 users not shown)
Line 2: Line 2:
{{Wegener's granulomatosis}}
{{Wegener's granulomatosis}}


{{CMG}}; '''Associate Editor-In-Chief:''' {{CZ}}
{{CMG}}{{APM}}{{AE}}{{KW}}{{CZ}}{{ADS}}


==Overview==
==Overview==
Obtaining a complete history is an important aspect in making a clinical diagnosis of Granulomatosis with polyangiitis. As it can help aid in differentiating between the ANCA associated vacuities and other possible causes that may mimic the disease.There are many similarities that are present between ANCA associated vacuities and Granulomatosis with polyangiitis. A history and physical can help assess the disease.
The symptomatology depends on the system involved. The disease involve ear nose and throat and cause symptoms of [[Sinusitis]], nasal crusting[[Otitis media|, otitis media]], [[Otorrhea]][[Epistaxis|, epistaxis]]. Patients with history of lung involvement presents with [[Hoarseness]], [[Cough]], [[Dyspnea]], [[Stridor]], [[Hemoptysis]]. Renal involvement presents with cloudy urine with [[hematuria]], [[edema]].


==Symptoms==
==History and Symptoms==
Obtaining a complete history is an important aspect in making a clinical diagnosis of Granulomatosis with polyangiitis. As it can help aid in differentiating between the ANCA associated vacuities and other possible causes that may mimic the disease. There are many similarities that are present between ANCA associated vacuities and Granulomatosis with polyangiitis. A history and physical can assess the disease.
Obtaining a complete history is an important aspect in making a clinical diagnosis of Granulomatosis with polyangiitis. As it can help differentiate between the ANCA associated vasculitis and other possible causes that may mimic the disease.  
The initial common signs that are present in patients with Granulomatosis with polyangiitis are non-specific in nature. The most common complaints are constitutional symptoms such as:<ref name="pmid6336643">{{cite journal| author=Fauci AS, Haynes BF, Katz P, Wolff SM| title=Wegener's granulomatosis: prospective clinical and therapeutic experience with 85 patients for 21 years. | journal=Ann Intern Med | year= 1983 | volume= 98 | issue= 1 | pages= 76-85 | pmid=6336643 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6336643  }} </ref>
* malaise
* pyrexia
* weight loss
* arthralgia
* cough
* dyspnea
* purpura
* abnormal urinary sediment


Ear, nose and throat involvement:
The initial symptomsthat are present in patients with Granulomatosis with polyangiitis are non-specific in nature. The following are history and symptoms of Granulomatosis with polyangiitis:<ref name="pmid13560836">{{cite journal| author=WALTON EW| title=Giant-cell granuloma of the respiratory tract (Wegener's granulomatosis). | journal=Br Med J | year= 1958 | volume= 2 | issue= 5091 | pages= 265-70 | pmid=13560836 | doi= | pmc=2026251 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=13560836  }}</ref><ref name="pmid2202308">{{cite journal| author=Leavitt RY, Fauci AS, Bloch DA, Michel BA, Hunder GG, Arend WP et al.| title=The American College of Rheumatology 1990 criteria for the classification of Wegener's granulomatosis. | journal=Arthritis Rheum | year= 1990 | volume= 33 | issue= 8 | pages= 1101-7 | pmid=2202308 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2202308  }} </ref><ref name="pmid6336643">{{cite journal| author=Fauci AS, Haynes BF, Katz P, Wolff SM| title=Wegener's granulomatosis: prospective clinical and therapeutic experience with 85 patients for 21 years. | journal=Ann Intern Med | year= 1983 | volume= 98 | issue= 1 | pages= 76-85 | pmid=6336643 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=6336643  }} </ref><ref name="pmid27733943">{{cite journal| author=Pagnoux C| title=Updates in ANCA-associated vasculitis. | journal=Eur J Rheumatol | year= 2016 | volume= 3 | issue= 3 | pages= 122-133 | pmid=27733943 | doi=10.5152/eurjrheum.2015.0043 | pmc=5058451 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27733943  }} </ref>
* nasal crusting
* sinusitis
* otitis media
* otorrhea
* epistaxis
* ulcers of the oral cavity or nasal
* conductive and or sensorineural hearing loss
* saddle nose deformity
* masses present in the upper airway
* cranial nerve entrapment


Pulmonary involvement:
'''Constitutional Symptoms'''
* hoarseness
* [[Malaise]]
* cough
* [[Pyrexia]]
* dyspnea
* [[Weight loss]]
* stridor
* [[Arthralgia]]
* hemoptysis
* [[Cough]]
* pulmonary fibrosis
* [[Dyspnea]]
* pulmonary arterial hypertension
* [[Purpura]]
* parenchymal lung nodules


Renal involvement:
'''Ear, nose and throat involvement:'''
* glomerulonephritis
* [[Sinusitis]]
* hematuria
* Nasal crusting
* rise in serum creatinine
* [[Otitis media]]
* edema
* [[Otorrhea]]
* hypertension
* [[Epistaxis]]
* red cell cast
* Ulcers of the oral cavity or nasal
* [[Conductive hearing loss|Conductive]] and or [[sensorineural hearing loss]]
* [[Saddle nose]] deformity
* Masses present in the upper airway
* Cranial nerve entrapment


Cutaneous involvement:
'''Pulmonary involvement:'''
* leukocytoclastic angiitis
* [[Hoarseness]]
* livedo reticularis
* [[Cough]]
* [[Dyspnea]]
* [[Stridor]]
* [[Hemoptysis]]
* [[Pulmonary fibrosis]]
* [[Pulmonary arterial hypertension]]
* Parenchymal lung nodules


Ophthalmic involvement:
'''Renal involvement:'''
* conjunctivitis
* [[Glomerulonephritis]]
* ulceration of the cornea
* [[Hematuria]]
* episcleritis
* Rise in [[serum creatinine]]
* [[Edema]]
* [[Hypertension]]


Nervous system involvement:
'''Cutaneous involvement:'''
* mononeuritis multiplex
* Leukocytoclastic angiitis
* sensory neuropathy
* [[Livedo reticularis]]
* sensorineural hearing loss
* pachymeningitis


'''Ophthalmic involvement:'''
* [[Conjunctivitis]]
* Ulceration of the [[cornea]]
* [[Episcleritis]]
'''Nervous system involvement:'''
* [[Mononeuritis multiplex]]
* [[Sensory neuropathy]]
* [[Sensorineural hearing loss]]
* [[Pachymeningitis interna|Pachymeningitis]]




Line 73: Line 73:
# the presence of anti-neutrophil cytoplasmic antibodies
# the presence of anti-neutrophil cytoplasmic antibodies
# the presence of glomerulonephritis
# the presence of glomerulonephritis


==References==
==References==
{{Reflist|2}}
{{Reflist|2}}


[[Category:Arthritis]]
[[Category:Arthritis]]

Latest revision as of 17:23, 11 April 2018

Granulomatosis with polyangiitis Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Granulomatosis with polyangiitis from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Chest X Ray

CT

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case Studies

Case #1

Granulomatosis with polyangiitis history and symptoms On the Web

Most recent articles

Most cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Granulomatosis with polyangiitis history and symptoms

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Granulomatosis with polyangiitis history and symptoms

CDC on Granulomatosis with polyangiitis history and symptoms

Granulomatosis with polyangiitis history and symptoms in the news

Blogs on Granulomatosis with polyangiitis history and symptoms

Directions to Hospitals Treating Granulomatosis with polyangiitis

Risk calculators and risk factors for Granulomatosis with polyangiitis history and symptoms

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]Cafer Zorkun, M.D., Ph.D. [4]Amandeep Singh M.D.[5]

Overview

The symptomatology depends on the system involved. The disease involve ear nose and throat and cause symptoms of Sinusitis, nasal crusting, otitis media, Otorrhea, epistaxis. Patients with history of lung involvement presents with Hoarseness, Cough, Dyspnea, Stridor, Hemoptysis. Renal involvement presents with cloudy urine with hematuria, edema.

History and Symptoms

Obtaining a complete history is an important aspect in making a clinical diagnosis of Granulomatosis with polyangiitis. As it can help differentiate between the ANCA associated vasculitis and other possible causes that may mimic the disease.

The initial symptomsthat are present in patients with Granulomatosis with polyangiitis are non-specific in nature. The following are history and symptoms of Granulomatosis with polyangiitis:[1][2][3][4]

Constitutional Symptoms

Ear, nose and throat involvement:

Pulmonary involvement:

Renal involvement:

Cutaneous involvement:

Ophthalmic involvement:

Nervous system involvement:


A diagnosis of Granulomatosis with polyangiitis can be made when three out of the six criteria are established. They are:[5]

  1. a histopathology that shows granuloma
  2. the upper respiratory tract is involved
  3. there is a stenosis that is present in larynx, trachea, and the bronchioles
  4. the pulmonary system is involved
  5. the presence of anti-neutrophil cytoplasmic antibodies
  6. the presence of glomerulonephritis

References

  1. WALTON EW (1958). "Giant-cell granuloma of the respiratory tract (Wegener's granulomatosis)". Br Med J. 2 (5091): 265–70. PMC 2026251. PMID 13560836.
  2. Leavitt RY, Fauci AS, Bloch DA, Michel BA, Hunder GG, Arend WP; et al. (1990). "The American College of Rheumatology 1990 criteria for the classification of Wegener's granulomatosis". Arthritis Rheum. 33 (8): 1101–7. PMID 2202308.
  3. Fauci AS, Haynes BF, Katz P, Wolff SM (1983). "Wegener's granulomatosis: prospective clinical and therapeutic experience with 85 patients for 21 years". Ann Intern Med. 98 (1): 76–85. PMID 6336643.
  4. Pagnoux C (2016). "Updates in ANCA-associated vasculitis". Eur J Rheumatol. 3 (3): 122–133. doi:10.5152/eurjrheum.2015.0043. PMC 5058451. PMID 27733943.
  5. Noone D, Hebert D, Licht C (2016). "Pathogenesis and treatment of ANCA-associated vasculitis-a role for complement". Pediatr Nephrol.   ( ):  . doi:10.1007/s00467-016-3475-5. PMID 27596099.

Template:WikiDoc Sources