1.Central Retinal Arterial Occlusion in Granulomatosis with Polyangiitis.
Kyu Young SHIM ; Sung Il SOHN ; Yu Cheol KIM
Korean Journal of Ophthalmology 2018;32(6):519-520
No abstract available.
Granulomatosis with Polyangiitis*
;
Retinaldehyde*
2.Eosinophilic Granulomatosis with Polyangiitis Diagnosed by Gallbladder Tissue.
WooSeong JEONG ; Changlim HYUN ; Jinsoek KIM
Journal of Rheumatic Diseases 2019;26(1):83-84
No abstract available.
Eosinophils*
;
Gallbladder*
;
Granulomatosis with Polyangiitis*
3.Frosted Branch Angiitis Secondary to Granulomatosis with Polyangiitis
Dong Yoon KIM ; Jinho JEONG ; Jin Young KIM
Korean Journal of Ophthalmology 2019;33(5):485-486
No abstract available.
Granulomatosis with Polyangiitis
;
Vasculitis
4.Granulomatosis with Polyangiitis Presenting as Cholangitis and Acute Kidney Injury
Chonnam Medical Journal 2019;55(2):124-125
No abstract available.
Acute Kidney Injury
;
Cholangitis
;
Granulomatosis with Polyangiitis
5.Facial Palsy with Tongue Ulcer: A Rare Initial Presentation of Granulomatosis with Polyangiitis
Ain Nabila Za&rsquo ; im Nur ; Mohd Shawal Firdaus Mohamad ; Noor Afidah Abdullah ; Geok Chin Tan ; Azman Mawaddah
Archives of Orofacial Sciences 2022;17(1):151-156
ABSTRACT
Granulomatosis with polyangiitis (GPA) is a rare multisystem disease. Although GPA is rare, it
commonly presents in a localised stage where its manifestation involves the upper or lower respiratory
tract before progressing to a generalised stage. Therefore, most patients with GPA will visit an oral
surgeon or an otolaryngologist to seek treatment. However, the diagnosis of GPA is often delayed as
GPA is not frequently considered as a differential diagnosis in common oral and facial diseases. The lack
of gold standard investigation for the diagnosis of GPA makes management of this case, a diagnostic
conundrum. We herein report a patient who was diagnosed with bilateral acute otitis media and left
mastoiditis complicated with facial nerve palsy, and later developed tongue ulceration one month after
his initial presentation. The ear, facial and oral symptoms represent a diagnostic red herring to a full-blown generalised stage of GPA.
Facial Paralysis
;
Oral Ulcer
;
Granulomatosis with Polyangiitis
6.A Case of Eosinophilic Granulomatosis with Polyangiitis Mimicking Cutaneous Tuberculosis and Tuberculous Lymphadenitis
Chang Wei Hsi ; Rajeswari A/P Gunasekaran ; Manisha Chandran ; Ng Fei Yin ; Ireen Razini Ab Rahman ; Ng Ting Guan
Malaysian Journal of Dermatology 2022;49(Dec 2022):20-24
Summary
Eosinophilic granulomatosis with polyangiitis (EGPA), or Churg-Strauss Syndrome (CSS) is a rare
granulomatous necrotizing vasculitic disease characterized by the presence of asthma, sinusitis, and
hypereosinophilia. We describe a patient who was initially diagnosed with tuberculous lymphadenitis
and later diagnosed with EGPA.
Granulomatosis with Polyangiitis
;
Tuberculosis, Cutaneous
;
Tuberculosis, Lymph Node
10.Eosinophilic Annular Erythema in a Patient with Eosinophilic Granulomatosis with Polyangiitis (Churg-Strauss Syndrome).
Ho Jeong SHIN ; Myoung Eun CHOI ; Woo Jin LEE
Korean Journal of Dermatology 2019;57(1):51-53
No abstract available.
Churg-Strauss Syndrome
;
Eosinophils*
;
Erythema*
;
Granulomatosis with Polyangiitis*
;
Humans
;
Hypereosinophilic Syndrome
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