Investigating the histopathological findings and immunolocalization of rickettsialpox infection in skin biopsies: A case series and review of the literature

• Published in: Journal of cutaneous pathology 2020-05, Vol.47 (5), p.451-458
• Main Authors: Vyas, Nikki S., Shieh, Wun‐Ju, Phelps, Robert G.
• Format: Article
• Language: English
• Subjects: Adult; Aged, 80 and over; Antigens, CD - metabolism; Antigens, CD20 - metabolism; Antigens, Differentiation, Myelomonocytic - metabolism; Biopsy; Biopsy - methods; CD20 antigen; CD3 antigen; CD3 Complex - metabolism; Dermis; Edema; Epidermis; Erythrocytes; Female; Fever; Fibrin; Histiocytes - pathology; Histopathology; HIV; HIV - isolation & purification; HIV Infections - complications; HIV Infections - diagnosis; HIV Infections - pathology; human immunodeficiency virus; Humans; immunohistochemistry; Immunohistochemistry - methods; Infections; Leukocytes (neutrophilic); Literature reviews; Male; Middle Aged; Necrosis; Necrosis - etiology; Necrosis - pathology; Peroxidase; Peroxidase - metabolism; Rickettsia akari; Rickettsia akari - immunology; Rickettsia akari - isolation & purification; rickettsial infection; Rickettsialpox; skin; Skin - pathology; Skin Diseases - microbiology; Skin Diseases - pathology; Spotted Fever Group Rickettsiosis - metabolism; Spotted Fever Group Rickettsiosis - microbiology; Spotted Fever Group Rickettsiosis - pathology; Vasculitis; Vasculitis - etiology; Vasculitis - pathology
• ISSN: 0303-6987; 1600-0560
• DOI: 10.1111/cup.13649

Background Recognition of rickettsialpox infection on skin biopsy can be challenging. The histopathology is non‐specific and inconsistently described. We assess classic histopathologic features in confirmed cases and review the literature. Methods We searched for cases of “rickettsialpox” diagnosed between 2006 and 2018 with positive immunostaining for Spotted Fever Group Rickettsia species. Original slides were evaluated for vacuolar alterations, granulomatous inflammation, vasculitis, necrosis, fibrin thrombi, microvesiculation, papillary dermal edema, and extravasated red blood cells. All biopsies were stained for CD3, CD20, CD68, and myeloperoxidase. Results Six biopsy specimens were compiled, three of which were sampled from vesiculopapules, one from a maculopapule, and two from eschars. Vacuolar alterations and vasculitis were present in all specimens (6/6; 100%). Granulomatous inflammation was present in five specimens (5/6; 83.3%). Fibrin thrombi and red blood cells were seen in 3/6 (50%) of specimens. The eschars showed necrosis of the epidermis and superficial dermis (2/6, 33.3%). Only one specimen showed intraepidermal vesiculation and papillary dermal edema (1/6; 16.7%). All six specimens showed perivascular infiltration with CD3+ T‐cells, and low amounts of CD20+ B‐cells and neutrophils. Five of the six specimens (83.3%) showed significant levels of CD68+ histiocytes. Conclusion The histopathology of rickettsialpox infection is septic lymphocytic and granulomatous vasculitis.