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Introduction: First described by Brunsting et al in 1930. Pyoderma
gangrenosa is an ulcerative disorder of unknown etiology,
which is characterised by neutrophilic infiltration of deep dermis
along with necrosis and ulceration of overlying epithelium. Association
of pyoderma has been described with many conditions
like, inflammatory bowel disease, lymphoma, autoimmune disorder
as well drug associated. Although previously described due
to bacterial infection but recent study shows that immune dysregulation
and abnormal neutrophilic function is main pathogenesis
of pyoderma gangrenosa. Pyoderma gangrenosa is very rare
in renal transplant patient; here we describe a case report who
presentation is typical of pyoderma gangrenosa both clinically
and histopathologically.
Case Report: A 33 years old woman underwent a donor nephrectomy
in March 2019. Three to four days after the surgical
site closure she developed a small pustular lesion over the surgical
site. General condition of the patient was stable, oriented to
time, place and person. Her vitals, pulse and temperature were
within normal limits. Investigation show increased in total leukocytes
counts (24000/ microliter) with differential count within
normal distribution. Platelets count was also within normal range.
Her renal graft function was appearing to stable with urea and
creatinine level of 22 mg/dl and 0.8 mg/dl respectively.
On muco-cutaneous examination, there was involvement of the
left side of abdomen just over the surgical site mark. The lesion
was in the form of well-defined deep ulcer with a necrotic slough and bluish undermined edge and violaceous margin. There was
surrounding induration. Significant tenderness was also present.
No satellite lesion or pathergy noted. Histopathological examination
shows stratified squamous epithelial lining with areas of
ulceration and necrosis and neutrophilic exocytosis. The underlying
dermis shows dense inflammatory cell infiltrate comprises of
predominantly neutrophils. There is peri appendageal neutrophilic
infiltration.
For this lesion, she received oral and IV antibiotic but did not respond.
After that, she also underwent surgical debridement twice
with a diagnosis of surgical site infection. After skin biopsy, she
started with steroid and lesion improve with steroid treatment.
Conclusion: To conclude, pyoderma gangrenosa in post donor
nephrectomy patient is very rare, with diagnosis confirmed by
clinically and histopathologically and exclusion of other factor
Biography
Dr. Gyanendra Singh completed his MD Pathology from Institute of Medical Sciences, BHU, Varanasi India, which is one of the prestigious medical colleges in India. He also completed his three-year senior residency and one year fellowship. He completed his research in field of diabetes. He developed this approach based on his years of experience working in hospitals and educational institutions in research, evaluation, teaching, and administration.
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