Commentary - (2025) Volume 12, Issue 1
Received: 28-Jan-2025, Manuscript No. JPD-25-168983;
Editor assigned: 31-Jan-2025, Pre QC No. P-168983;
Reviewed: 11-Feb-2025, QC No. Q-168983;
Revised: 18-Feb-2025, Manuscript No. R-168983;
Published:
25-Feb-2025
, DOI: 10.37421/2684-4281.2025.12.502
Citation: Hailee, Edith. “Rare Dermatologic Presentations in Immunocompromised Individuals: Case Series and Review.” J Dermatol Dis 12 (2025): 502.
Copyright: © 2025 Hailee E. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.
In another case, a 29-year-old male with advanced HIV infection presented with extensive verrucous plaques on the face and neck, mimicking hypertrophic warts or cutaneous malignancy. Histopathology and PCR confirmed disseminated histoplasmosis with cutaneous involvement, a rare presentation of a fungal infection endemic to certain regions. The cutaneous lesions responded to intravenous liposomal amphotericin B followed by itraconazole. This case emphasized the importance of considering systemic mycoses in patients with low CD4 counts, even when lesions appear localized to the skin. A third patient, a 38-year-old woman undergoing chemotherapy for acute leukemia, developed painful, hemorrhagic bullae and dusky plaques over her extremities. Differential diagnosis included Stevens-Johnson syndrome, vasculitis and neutrophilic dermatoses. Skin biopsy revealed dermal infiltration with atypical myeloid cells, consistent with leukemia cutis. This rare presentation highlights how hematologic malignancies can directly infiltrate the skin, masquerading as infectious or inflammatory dermatoses. Early dermatopathologic evaluation is essential, especially when the lesions deviate from expected chemotherapy-associated reactions [2].
Another rare but critical presentation involved a 54-year-old liver transplant recipient who developed multiple non-healing ulcers and nodules over the scalp and trunk. The clinical picture resembled pyoderma gangrenosum, but biopsy demonstrated atypical keratinocytes and viral inclusions. Immunohistochemistry and in situ hybridization confirmed cutaneous squamous cell carcinoma (SCC) with human papillomavirus (HPV) positivity. Immunosuppressed individuals, particularly transplant recipients, are at significantly increased risk for aggressive cutaneous malignancies, especially SCC, which tends to occur in multiple sites and with increased recurrence. This case reiterates the need for routine skin surveillance in chronically immunosuppressed patients and a high index of suspicion for malignancy when faced with atypical ulcers or nodules [1].
A particularly perplexing case involved a 62-year-old man with poorly controlled diabetes and chronic corticosteroid use for autoimmune disease who presented with targetoid lesions and mucosal erosions. The clinical suspicion was for erythema multiforme or drug reaction. However, subsequent biopsy revealed features of Kaposiâ??s sarcoma, confirmed by positive HHV-8 immunostaining. Although classically associated with HIV, Kaposiâ??s sarcoma may also occur in iatrogenically immunosuppressed individuals, such as organ transplant recipients or those with autoimmune diseases. The lesions regressed after tapering immunosuppressive therapy and initiating systemic treatment with pegylated liposomal doxorubicin. One of the rarest cases observed was a 26-year-old female with systemic lupus erythematosus on azathioprine therapy who developed chronic, ulcerative lesions over the genital region. While herpes simplex virus (HSV) was suspected, the ulcers were unusually large and persistent. Viral culture confirmed HSV-2 and she was treated successfully with prolonged antiviral therapy. This case illustrates how viral infections in immunocompromised patients can present in exaggerated forms, with chronicity and resistance to standard durations of therapy.
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