1.Two cases of alopecia presenting with atypical features
Patricia Andrea L. Chua ; Maria Franchesca S. Quinio-Calayag
Journal of the Philippine Dermatological Society 2024;33(Suppl 1):8-8
This case series highlights the diagnostic challenges in differentiating between scarring and nonscarring alopecia, as both patients presented with similar features yet had distinct underlying conditions.
The first patient (60 year old, female) was initially diagnosed with Frontal Fibrosing Alopecia due to the pattern of hair loss in the frontal area of the scalp. Trichoscopy shows perifollicular and interfollicular scaling, yellow crusts around the follicles, dotted vessels, yellow structureless areas with surrounding erythema. However, the patient responded well to Clobetasol Propionate 500mcg/mL Scalp Solution twice a day and Minoxidil 5% Solution twice a day for 30 days, which was not expected in patients with scarring alopecia. Further evaluation revealed that the hair loss was due to Telogen Effluvium and Seborrheic Dermatitis.
In contrast, the second patient (54 year old, female), which was managed as a case of Discoid Lupus Erythematosus of the scalp. Trichoscopy shows absence of follicular opening, white patches, perifollicular scale, white and brown dots. Despite receiving similar treatment, the patient did not experience any improvement, reinforcing the complexity of managing hair loss disorders.
A key aspect of this case series is the emphasis on Trichoscopy. It shows specific patterns associated with various types of alopecia, allowing for prompt diagnosis and treatment while reducing the need for unnecessary biopsies. It invites further discussion on the importance of accurate assessment, the role of Trichoscopy in diagnosis, and the potential for unexpected responses to treatment in Dermatology.
Human ; Female ; Middle Aged: 45-64 Yrs Old
2.Breaking boundaries: A case report on the use of ultrasound-guided sclerotherapy with bleomycin for rare pediatric vulvar lymphangioma
Madelaine Johanna L. Abraham ; Dee Jay B. Arcega ; Maria Franchesca S. Quinio-Calayag
Journal of the Philippine Dermatological Society 2024;33(Suppl 1):32-32
Lymphangioma is a rare vascular malformation, comprising about 4% of such anomalies. Its most common symptom is swelling, which often leads to cosmetic deformity. The most prevalent subtype, lymphangioma circumscriptum, seldom presents on the vulvar area, making treatment especially challenging due to potential complications and recurrence risks.
This is a case of a 10-year-old Filipino female, otherwise healthy, who presented with progressively enlarging, tender, “frog spawn”-like papules on the left vulva since birth. These papules showed partial improvement following surgical excision. Histopathological examination confirmed the diagnosis of lymphangioma. Over the past year, the patient experienced recurrence of papules, resulting in vulvar asymmetry and labial swelling. Pelvic magnetic resonance imaging (MRI), ultrasound, and fine needle aspiration biopsy, revealed multiple superficial and deep cystic masses consistent with lymphangioma. Long-pulsed Nd:YAG laser was administered to the external lesions, yielding partial improvement. Subsequently, she underwent ultrasound-guided sclerotherapy with bleomycin under local anesthesia.
This procedure, performed by interventional radiology, successfully resolved the deep cysts and swelling after two sessions, with no reported complications.
In cases of cutaneous lymphangioma, especially in anatomically sensitive regions like the vulva, imaging plays a crucial role in determining lesion depth and guiding treatment to minimize recurrences. Although no local literature is available, this case highlights the effectiveness and safety of ultrasound-guided sclerotherapy with bleomycin as a novel treatment option for lymphangioma.
Human ; Female ; Child: 6-12 Yrs Old ; Lymphangioma ; Sclerotherapy
3.Efficacy and safety of platelet-rich plasma using acid citrate dextrose solution A versus sodium citrate PRP kit in treating adult pattern hair loss: A single blind, randomized, placebo-controlled, equivalence trial
Kelsie Kirsty C. Santos ; Maria Franchesca S. Quinio-Calayag ; Fatima Dc. Jacinto-Calimag
Journal of the Philippine Dermatological Society 2024;33(Suppl 1):43-44
BACKGROUND
Despite the widespread prevalence of pattern hair loss, treatment options remain limited. Platelet-rich plasma (PRP) is a promising alternative but is hindered by high costs and a lack of standardized protocols. In the Philippines, only one FDA-approved PRP kit is available, leading to interest in whether Acid Citrate Dextrose Solution A (ACD-A) tube could provide equivalent results. Additionally, international research on different anticoagulant preparations is lacking, with no studies conducted in the Philippines.
OBJECTIVETo determine if the efficacy and safety of PRP therapy using ACD-A and Sodium Citrate (SC) PRP Kit are equivalent in the treatment of adult pattern hair loss.
METHODSA single-blind, randomized, placebo-controlled, equivalence trial. Participants were randomly assigned to either a control group or a treatment group receiving ACD-A or SC PRP Kit preparations. Treatments were administered monthly for six sessions. Hair growth was assessed at baseline and after each session using global photography, hair classification system, and trichoscopy.
RESULTSA total of 48 participants completed the study, divided into three groups of 16 participants each. Mean hair density scores for the ACD-A and SC KIT groups, along with 95% confidence intervals for mean differences at various timeframes, fell within the equivalence margin of ±16 hair follicles/cm2. Minimal adverse effects were observed throughout the study.
CONCLUSIONACD-A produces results equivalent to the SC PRP Kit in terms of hair growth and patient satisfaction. Both preparations are safe, with only minor adverse effects, making ACD-A a viable alternative for PRP treatments of pattern hair loss.
Human ; Platelet-rich Plasma
4.Evaluation of the accuracy of dermoscopy as a point-of-care tool in the diagnosis of distal subungual onychomycosis in a tertiary hospital
Gemmy P. David ; Arunee H. Siripunvarapon ; Maria Angela M. Lavadia ; Maria Franchesca S. Quinio-Calayag ; Athena Emmanuelle P. Mallari
Journal of the Philippine Dermatological Society 2024;33(Suppl 1):33-34
BACKGROUND
Accurate diagnosis of onychomycosis is important because its treatment is long-term, costly, and sometimes with complications. KOH test is quick and cheap but has low sensitivity. Hence, the need for additional tests such as culture and/or PAS. However, these two tests are not readily available and expensive. Dermoscopy is an emerging tool for the diagnosis of nail conditions.
OBJECTIVEThis study aims to evaluate the accuracy of dermoscopy as a point-of-care tool in diagnosing distal subungual onychomycosis (DSO).
METHODSThis is a prospective, cross-sectional study of 22 clinically diagnosed DSO patients selected via convenience sampling in a tertiary hospital from November 2019 to March 2021. Participants had gross nail examination, dermoscopy, KOH and PAS tests. Measures of diagnostic accuracy for the different dermoscopic patterns were obtained, with KOH and PAS results as reference standard.
RESULTSFifty-one nail samples were submitted for processing with only 49 nails accepted for analysis. The most common pattern was jagged edge with spikes (65.3%). Combining all 5 dermoscopic patterns increased the sensitivity to 91.2% (95% CI: 76.3, 98.1).
CONCLUSIONSDermoscopy may be used as a first-step, point-of-care tool in the diagnosis of DSO. Addition of mycological and histopathological tests is still warranted for confirmation.
Dermoscopy ; Onychomycosis ; Potassium Hydroxide
5.One mistake, one life at stake: A case of Methotrexate Toxicity in A 57-Year old male presenting with painful plaques with erosions
Maria Franchesca S. Quinio ; Elizabeth P. Prieto
Journal of the Philippine Medical Association 2017;95(2):48-53
Introduction:
Methotrexate is being given by dermatologists in only extreme cases of skin disorders such as in severe Psoriasis Vulgaris. Strict precautionary measures are done to avoid its well-known adverse effects. An early but less common sign of its toxicity are painful erosions on plaques. Methotrexate is an effective but potentially toxic treatment for different severe dermatologic disorders such as in severe Psoriasis Vulgaris. Meticulous and complete history-taking, physical examination and laboratory work-up to come up with a correct diagnosis as well as, knowledge of indications for treatment, proper dosing, folate supplementa-tion, monitoring, proper referral and early detection of its toxicity are important in order to avoid cutaneous and systemic adverse effects including death.
Case Report
A case of a 57-year old male with a 2-day history of painful erosions on plaques on both upper and lower extremities after eleven days of taking Methotrexate 2.5mg/tablet one tablet three times a day without folate supplementation. He was then being treated by a general physician as a case of Psoriasis Vulgaris. He was subsequently admitted under the Internal Medicine service due to epigastric pain, nausea, anorexia, generalized body weakness and passage of black tarry stools. He was referred to the Department of Dermatology for the painful erosions on plaques. He expired two days after admission due to Acute Respiratory Failure. Post-mortem Skin punch biopsy was done and revealed chronic eczematous dermatitis consistent with Lichen Simplex Chronicus with superimposed drug induced hypersensitivity reaction.
Neurodermatitis
6.Lupus panniculitis in an ANA-negative systemic Lupus Erythematosus patient: A case report
Ma. Corazon A. Iniego-Rodas ; Maria Franchesca Quinio ; Charlene Ang-Tiu
Journal of the Philippine Dermatological Society 2021;30(1):45-48
Introduction:
Lupus panniculitis (LP) is an unusual type of cutaneous lupus erythematosus (CLE) wherein the cutaneous inflam-
matory reaction involves primarily the deeper dermis and subcutaneous fat. It is characterized by the appearance of recurrent,
mostly asymptomatic, firm, nodules or plaques, involving the face, upper limbs, and buttocks.
Case report:
In our case, a 30-year-old female presented with a non-tender, non-movable nodule on the left breast, 6 weeks
prior to her admission. She had fever, chills, and joint pains. The patient later developed hyperpigmented plaques on the infra-
clavicular area, and left flank extending to the abdomen. Urinalysis showed proteinuria, and RBC cast. She also had leukopenia,
and anemia on CBC. Chest computerized tomography (CT) scan revealed a heterogeneously enhancing soft tissue mass in the
base of the neck at the right infraclavicular region with malignant features. ANA titer was normal, while skin biopsy on two sites
and direct immunofluorescence studies were compatible with lupus panniculitis. She was managed as a case of systemic lupus
erythematosus (SLE) using a combination of hydroxychloroquine, and oral corticosteroids, which afforded temporary relief of
symptoms. The patient however was lost to follow-up and opted for alternative medicine, and subsequently succumbed to the
complications of SLE.
Conclusion
This case highlights the importance of a carefully made assessment after an accurate clinicopathological cor-
relation was done. This case also emphasizes that although LP if associated with SLE may signify a milder condition, judicious
monitoring and follow-up must still be undertaken since management is based on the disease activity.
Panniculitis, Lupus Erythematosus
7.Multiple neurofibromas with hypertrichosis in a Filipino patient with neurofibromatosis 1.
Leah Antoinette M. CARO-CHANG ; Maria Franchesca S. QUINIO ; Georgina C. PASTORFIDE
Acta Medica Philippina 2019;53(2):186-190
This is a case of an 11-year-old male who presented with multiple neurofibromas with hypertrichosis. Classic cutaneous neurofibromas, café-au-lait macules, axillary freckling, Lisch nodules, and scoliosis were also present fulfilling a diagnosis of Neurofibromatosis type 1. This is the first report of multiple neurofibromas with hypertrichosis in the Philippines. Hypertrichosis overlying a neurofibroma is rarely reported and the mechanism remains to be elucidated.
Human ; Neurofibromatosis 1 ; Hypertrichosis ; Neurofibroma