Pyoderma Gangrenosum



Fig. 27.1
A right leg ulcer in a 20-year-old male that originated from initial abrasion. He has no systemic disease



A304095_1_En_27_Fig2_HTML.jpg


Fig. 27.2
The ulcer expanded with a purulent and necrotic base even though ointment was used


Pathergy is a specific but not sensitive finding of PG. The lesion sites expand radically, especially if the borders of the lesion site are traumatized by debridement or by other mechanical trauma [3]. No laboratory finding is diagnostic of PG. PG has no definite diagnostic criteria and is a diagnosis of exclusion. The diagnosis of PG is very difficult and based primarily on the clinical history, clinical manifestation, and biopsy result while being careful about misdiagnosis (Table 27.1). [1, 2, 6]


Table 27.1
Causes of ulcers mimicking PG



































Infection

Fungal

Mycobacterial

Necrotizing fasciitis

Vascular occlusive disease

Antiphospholipid-antibody syndrome

Venous stasis ulceration

Vasculitis

Wegener’s granulomatosis

Polyarteritis nodosa

Neoplasms

Lymphoma

Leukemia cutis

Drug reactions

Hydroxyurea induced ulcer



27.4 Treatments


If the patients have a systemic disease, the systemic disease should be preferentially treated. It is difficult to get cured completely by local wound management alone. Topical treatments are chosen depending on the purpose such as the prevention of secondary bacterial infection or the promotion of reepithelialization. Some topical agents such as tacrolimus, strong corticosteroids, and cyclosporine have reported efficacy in small case series. PG is commonly treated with systemic corticosteroids and/or cyclosporine [7].

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Nov 3, 2016 | Posted by in Dermatology | Comments Off on Pyoderma Gangrenosum

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