Literature DB >> 36042972

Chronic superficial ulcers on the trunk.

Alli J Blumstein1, Sagar Patel1, Kiran Motaparthi1.   

Abstract

Entities:  

Keywords:  PG, pyoderma gangrenosum; SGP, superficial granulomatous pyoderma; chronic ulcer; pyoderma gangrenosum; superficial granulomatous pyoderma

Year:  2022        PMID: 36042972      PMCID: PMC9420335          DOI: 10.1016/j.jdcr.2022.07.023

Source DB:  PubMed          Journal:  JAAD Case Rep        ISSN: 2352-5126


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Case

A 62-year-old man presented with several painful superficial ulcers on the trunk that began to expand slowly 1 year after inguinal hernia surgery. Physical examination demonstrated 5 ulcerative plaques on a violaceous base with overlying crust (Figs 1 and 2). A punch biopsy was performed, and tissue bacterial, fungal, and acid-fast bacilli cultures demonstrated no growth.
Fig 1
Fig 2
Question 1: Which of the following is the best diagnosis? Superficial granulomatous pyoderma (SGP) Ecthyma Blastomycosis-like pyoderma Chromomycosis Factitious ulcer Answer: SGP – Correct. SGP is an uncommon variant of pyoderma gangrenosum (PG) characterized by slowly progressive superficial ulcers with vegetative margins and a clean granulating base. Unlike classic PG, SGP most commonly occurs on the trunk and is not significantly associated with systemic conditions. Ecthyma – Incorrect. Ecthyma is a deep, ulcerative version of impetigo that is characterized by punched-out ulcers, most commonly observed on the lower extremities. The most commonly implicated bacteria include Streptococcus pyogenes and Staphylococcus aureus. Blastomycosis-like pyoderma – Incorrect. Blastomycosis-like pyoderma is characterized by large verrucous plaques with pustules and an elevated border and is most commonly observed on the distal extremities. Chromomycosis – Incorrect. Chromomycosis most often presents as a solitary verrucous nodule or plaque on an acral anatomic site. Factitious ulcer – Incorrect. Factitious ulcers often demonstrate irregular or geographic borders and are induced by patients who assume the sick role without secondary gain. Question 2: What is the most common anatomic site observed in this disorder? Trunk Extremities Face Anogenital region Head and neck Answer: Trunk – Correct. SGP most commonly occurs on the trunk. Disseminated disease affects multiple anatomic sites. Extremities – Incorrect. Classic ulcerative PG typically affects the lower extremities. Face – Incorrect. While SGP is rarely reported on the face, this is not the most common anatomic site. SGP on the face appears to be refractory to topical and systemic corticosteroids. Anogenital region – Incorrect. The anogenital region is rarely described in SGP. Hands and neck – Incorrect. This is not a typical location for SGP. Question 3: Which of the following descriptions reflects the histopathologic findings in this disorder? Necrotic epidermis, ulcer, and sparse inflammation Pigmented yeast with internal transverse septae Ulceration with dense neutrophilic infiltrate and dermal necrosis Layered suppurative granuloma with necrosis and suppuration surrounded by histiocytes and plasma cells, along with overlying epidermal hyperplasia Pseudoepitheliomatous hyperplasia with neutrophilic abscesses and scar-like fibrosis Answer: Necrotic epidermis, ulcer, and sparse inflammation – Incorrect. These are nonspecific findings typically observed in factitious ulcer. Pigmented yeast with internal transverse septae – Incorrect. Medlar or sclerotic bodies undergo binary fission and are characteristic of chromomycosis. Ulceration with dense neutrophilic infiltrate and dermal necrosis – Incorrect. This describes findings present in classic ulcerative PG, which lacks the layered suppurative granuloma typical of SGP.1, 2, 3, 4 Layered suppurative granuloma with necrosis and suppuration surrounded by histiocytes and plasma cells, along with overlying epidermal hyperplasia – Correct. While nonspecific, these findings are consistent in SGP.1, 2, 3, 4 Pseudoepitheliomatous hyperplasia with neutrophilic abscesses and scar-like fibrosis – Incorrect. Blastomycosis-like pyoderma demonstrates these features; isolation of a pathogenic organism such as Staphylococcus aureus is required for diagnosis.

Conflicts of interest

None disclosed.
  4 in total

Review 1.  Superficial granulomatous pyoderma: a case in an 11-year-old girl and review of the literature.

Authors:  Megha M Tollefson; Robert H Cook-Norris; Amy Theos; Dawn M R Davis
Journal:  Pediatr Dermatol       Date:  2010 Sep-Oct       Impact factor: 1.588

2.  Superficial granulomatous pyoderma.

Authors:  A L Schroeter
Journal:  Mayo Clin Proc       Date:  1989-01       Impact factor: 7.616

3.  Superficial Granulomatous Pyoderma Successfully Treated with Intravenous Immunoglobulin.

Authors:  Sarah Borg Grech; Andrea Vella Baldacchino; Roberto Corso; David Pisani; Michael J Boffa
Journal:  Eur J Case Rep Intern Med       Date:  2021-09-09

Review 4.  Superficial Granulomatous Pyoderma Gangrenosum Involving the Face: A Case Series of Five Patients and a Review of the Literature [Formula: see text].

Authors:  Eran Shavit; Michael Cecchini; James J Limacher; Scott Walsh; Ashely Wentworth; Mark Denis P Davis; Afsaneh Alavi
Journal:  J Cutan Med Surg       Date:  2021-02-05       Impact factor: 2.092

  4 in total

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