1.Erythrokeratodermia variabilis et progressiva in a Filipino Girl: A case report
Maria Lourdes H. Palmero ; Franchesca Marie D. Ilagan
Journal of the Philippine Dermatological Society 2020;29(2):67-72
Introduction: Erythrokeratodermia variabilis et progressiva (EKVP) is a rare, usually autosomal dominant disorder characterized by co-existence of erythematous to hyperpigmented scaly plaques and stationary or migratory patches symmetrically distributed on the face, buttocks and extremities.
Case summary: This report describes an 8-month-old Filipino female infant who initially presented at 13 days old with erythematous scaly patches on the scalp, periorbital, perioral, and genital areas. These patches progressed to multiple erythematous plaques with well-defined erythematous to hyperpigmented border, some topped with hemorrhagic and yellowish crusts and scales on the scalp, face, neck, upper and lower extremities, genital and gluteal area. Histologic examination of the skin showed dense aggregates of neutrophils in the stratum corneum, parakeratosis, mild spongiosis, and irregular acanthosis. There were focal areas of hypogranulosis underneath the areas of parakeratosis; however, other areas showed normal granular cell layer. The dermis showed moderate superficial perivascular lymphohistiocytic cell infiltrates with melanophages. Histopathologic changes were nonspecific but may be consistent with EKVP. Patient was initially treated with IV antibiotics; however lesions continued to progress. She was then started on oral acitretin, resulting to improvement of lesions.
Conclusion: A Filipino girl with erythrokeratodermia variabilis et progressiva is reported. The knowledge of this disease and its treatment will allow clinicians to promptly initiate treatment and monitor treatment side effects
Erythrokeratodermia variabilis
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2.70-year-old Filipino male with primary cutaneous follicle center lymphoma: A case report
Marc Kristoffer C. Verdan ; Franchesca Marie D. Ilagan ; Eleanor L. Letran ; Patricia J. Ong ; Jc Kenneth M. Jacinto
Journal of the Philippine Dermatological Society 2024;33(Suppl 1):29-29
Primary cutaneous lymphoma are non-Hodgkin lymphomas with no evidence of extracutaneous disease. Classified into cutaneous T-cell lymphoma and cutaneous B-cell lymphoma from the WHO-EORTC classification 2018. 10 cases per million inhabitants per year worldwide are seen, wherein 20-25% are primary cutaneous B-cell lymphomas, with PCFCL having 12% frequency. Only 17 cases of cutaneous B cell lymphoma are recorded in the Philippines from 2011 to 2023. This rare case will add to the minimal data on the disease in the Philippines.
A 70-year old, Filipino male presenting with nodules, papules and plaques on the nose, forehead, preauricular areas, and temples of the face. Histopathologically, it showed atypical lymphoid follicles which were positive for CD20 and Bcl6 and negative for Bcl2, MUM-1, Cyclin D1, CD10 and CD5. Since there was no extracutaneous involvement, the final diagnosis was Primary Cutaneous Follicle Center Cell Lymphoma. He was treated with external beam radiation therapy with complete response, and no recurrence seven months after radiation therapy.
PFCL presents as papules, plaques, or tumors with a predilection for the scalp, forehead, and posterior torso. On dermoscopy, salmon-colored area and pro-eminent serpentine vessels, some having white circles with scales and arborizing vessels. Histologically, it expresses CD20 and Bcl-6, and predominantly Bcl-2 negative, but some cases show positive cells. Imaging and work-up ruled out systemic involvement Local radiation shows a close to 100% response rate.
PCFCL is still a rare disease nationwide.
Human ; Male ; Aged: 65-79 Yrs Old
3.Efficacy and safety of sunflower oil for mild to moderate plaque-type psoriasis: A double-blind, randomized controlled trial.
Franchesca Marie D. ILAGAN ; Eleanor L. LETRAN ; Bernardita O. POLICARPIO
Journal of Medicine University of Santo Tomas 2021;5(2):755-773
Background: Psoriasis is a chronic, complex, inflammatory disease that needs safe and effective treatment options to decrease its disease burden.
Objectives: To determine the efficacy and safety of sunflower oil in mild to moderate plaque-type psoriasis at the outpatient department of a tertiary hospital.
Methods: This was an 8-week, single-center, randomized, double-blind controlled trial that compared the efficacy and safety of sunflower oil + placebo cream (Group SO), betamethasone valerate cream + placebo oil (Group BC), sunflower oil + betamethasone valerate cream (Group SOBC) in mild to moderate plaque-type psoriasis. Psoriasis Area Severity Index (PASI) was used to measure the extent of psoriasis by assessing the erythema, induration, scaling, and body surface area involvement. The difference from baseline PASI was recorded. The Dermatology Life Quality Index (DLQI) questionnaire was used to measure the impact of psoriasis on the patient's quality of life.
Results: Fifty-one patients were randomized and blinded to three treatment arms; evaluated at baseline, week 4 and 8. The proportion of patients who achieved PASI ?50 at week 4 was 29% in Group SO, 38% in Group BC, and 60% in Group SO-BC. By week 8, Groups SO and BC achieved 80% while Group SO-BC achieved 93%. There was significant decline of PASI at week 4 and week 8 compared to baseline. The mean percentage change of PASI was highest at Group SO-BC followed by Group BC and lastly Group SO at week 4 and week 8. The mean reduction in score for scaling was significantly higher in Group SO-BC. Mean reduction in induration and erythema was not statistically significant across the three groups. There was 40-50% improvement in DLQI scores in all groups. There were no adverse events.
Conclusion: This study showed that sunflower oil is effective and safe in mild to moderate plaque-type psoriasis.
Sunflower Oil ; Randomized Controlled Trial ; Psoriasis