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1.
PAFMJ-Pakistan Armed Forces Medical Journal. 2017; 67 (1): 166-170
em Inglês | IMEMR | ID: emr-186454

RESUMO

Objective: To determine the frequencies of nasal itching, epistaxis, dry/chapped lips and xerosis of skin among Pakistani peacekeepers exposed to the dry climate of Nyala, Sudan


Study Design: Prospective cohort study


Place and Duration of Study: Pakistan Field Hospital 6 Nyala, Sudan, from February 2014 to May 2012


Material and Methods: Total 144 United Nations Pakistani Peacekeepers of Pakistan Field Hospital 6[all ranks] were selected by non-probability convenient sampling. The data consists of frequency of four symptoms was collected after three months of exposure to dry climate


Results: The most common symptom was dryness of skin [36.1%] followed by chapping of lips [29.9%] while nasal bleeding [epistaxis] was least common [9%]. Significantly higher number of subjects of ages more than 40 years had nasal bleeding compared to the younger group [p value 0.002]


Conclusion: Exposure to extreme dry climate affects skin and nasal mucosa. Frequency of epistaxis found to be significantly more in subjects older than 40 years as compared to younger ones

2.
JPAD-Journal of Pakistan Association of Dermatologists. 2017; 27 (1): 59-63
em Inglês | IMEMR | ID: emr-192287

RESUMO

Objective To compare the clinical efficacy of trichloroacetic acid [TCA] 100% and cryotherapy in xanthelasma palpebrarum [XP]


Methods 40 patients fulfilling the inclusion criteria were treated with cryotherapy on right eye [group A] and TCA on left eye [group B]. Patients were followed up for 6 weeks and final outcome variable of efficacy i.e. complete resolution of xanthelasma was assessed at 6 weeks. Adverse side effects of therapy were also recorded as secondary outcome variables. Data were analyzed by SPSS 19.0


Results Mean age of patients was 43.75 +/- 5.90 years and age ranged from 34 to 56 years. Out of 40 patients 9 [22.5%] were male and 40 [77.5%] were female. Complete resolution of xanthelasma was seen in only 7 [17.5%] in group A, while complete resolution of lesions was seen in 30 [75%] of patients in group B [p = 0.000]


Conclusion A single session of 100% TCA is highly effective than cryotherapy in the treatment of Xanthelasma palpebrarum

3.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2017; 27 (4): 200-202
em Inglês | IMEMR | ID: emr-189272

RESUMO

Objective: To compare the mean Vitamin D level in patients with alopecia areata [AA] with age and gender controlled matched healthy controls


Study Design: Case-control study


Place and Duration of Study: Dermatology OPD, JPMC, from October 2014 to March 2015


Methodology: All the patients diagnosed of alopecia areata by a trained dermatologist were selected. Controls were age and gender matched healthy volunteers. Venous blood was drawn and sent to hospital laboratory for 25 [OH] vitamin D by enzyme immunoassay method on chemical analyser. Data was recorded on SPSS version 16. Mann-Whitney test was applied to compare vitamin D levels of cases and controls. P-value <0.05 was taken as significant


Results: There are 30 cases of AA, and 30 age and gender matched controls. The mean age of our study group was 23.77 +/- 8.86 ng/dL in patients and 24.03 +/- 8.62 ng/dL in the control group. Fifteen [50%] patients presented between 3-12 months of onset of AA. Median [IQR] vitamin D level of cases was 13.5 [18.6] ng/dL and healthy controls was 22.5 [16.25] [p=0.001]


Conclusion: Serum Vitamin D levels were significantly lower in patients with alopecia areata compared to healthy controls


Assuntos
Humanos , Masculino , Feminino , Adolescente , Adulto , Pessoa de Meia-Idade , Alopecia em Áreas , Vitamina D/sangue , Fatores Etários , Estudos de Casos e Controles , Identidade de Gênero
4.
JPAD-Journal of Pakistan Association of Dermatologists. 2016; 26 (1): 53-57
em Inglês | IMEMR | ID: emr-180960

RESUMO

Objective: To determine the frequency and pattern of cutaneous diseases among peacekeepers at a tertiary care hospital in United Nations and African Mission in Darfur, Sudan


Methods: This descriptive study was conducted at dermatology outpatient department of United Nations peacekeeping mission [UNAMID] level III Hospital at Darfur, Sudan from March 2014 to Feb 2015.Peacekeepers of both gender reporting to dermatology OPD were registered after informed consent. Patients' demographic profile, nature of duty, disease diagnosis and duration of illness were noted. The data was managed and analyzed using SPSS-17


Results: A total of 542 peacekeepers of the age ranging from 20-60 years were analyzed. Eczema was the most common disease [38.7%], followed by fungal infections [22.5%] and acne [10.7%]. 47.6% of patients had the disease before deployment in mission area and 52.4% developed after reaching in mission area


Conclusion: Eczema, dermatophytosis and acne were the commonest skin problems among peacekeeper. Almost half of these had dermatological problems before deployment

5.
JPAD-Journal of Pakistan Association of Dermatologists. 2016; 26 (1): 80-82
em Inglês | IMEMR | ID: emr-180966

RESUMO

Bullous pemphigoid [BP] is an autoimmune subepidermal blistering condition that predominantly affects older patients and characterized by local or generalized tense blister formation. Mucosal involvement with small blisters or erosions may exist in a minority of patients. BP is generally self-limiting with remission in most patients by 5 years. We report an 83-year-old hemiplegic lady with unusual distribution of bullous pemphigoid lesions

6.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2016; 26 (6): 545-546
em Inglês | IMEMR | ID: emr-182338
7.
JPAD-Journal of Pakistan Association of Dermatologists. 2016; 26 (4): 287-289
em Inglês | IMEMR | ID: emr-185952
8.
JPAD-Journal of Pakistan Association of Dermatologists. 2016; 26 (4): 306-309
em Inglês | IMEMR | ID: emr-185955

RESUMO

Objective To compare Tzanck smear with viral serology in terms of concurrence of results in patients with varicella


Methods It was a descriptive case-series done at Dermatology Department, Military Hospital, Rawalpindi. We studied 50 patients of the varicella infection in 6 months. Tzanck smear was taken from each patient at presentation and stained by Giemsa stain for giant cells and evaluated by histopathologist. Viral serology was done by complement fixation method at Virology Department. The results were statistically analyzed with SPSS 16


Results Out of 50 patients of varicella 39 [78%] were males while 11 [22%] were females. Mean age was 30.52 +/- 9.763 years. Tzanck smear was positive in 33 [66%] and viral serology in 45 [90%] patients. The concurrence of results in both Tzanck smear and viral serology was seen in 31 patients [62%]


Conclusion Tzanck smear is a quick and valuable tool in the diagnosis of patients suffering from varicella

9.
JPAD-Journal of Pakistan Association of Dermatologists. 2016; 26 (4): 383-385
em Inglês | IMEMR | ID: emr-185969

RESUMO

A 40-year-old male presented with generalized asymptomatic cutaneous infiltrated plaques involving trunk, Jimbs and face. He had acraJ sensory Joss along with symmetrical nerve thickening and enlargement. Slit-skin smear revealed multiple acid-fast bacilli [AFB] on Wade-Fite staining, thus confirming the diagnosis of lepromatous leprosy


Patient had a remarkable sparing of skin creases at various sites including trunk, antecubital fossa and axillary flexures suggestive of a positive [Deck Chair Sign]. This sign has been described in literature mostly in papuloerythroderma of Ofuji and other related dermatosis. To our knowledge this is the first case report of lepromatous leprosy with deck chair sign' from Pakistan

10.
PAFMJ-Pakistan Armed Forces Medical Journal. 2015; 65 (5): 649-652
em Inglês | IMEMR | ID: emr-176989

RESUMO

To determine the diagnostic accuracy of slit skin smears in clinically suspected patients of leprosy using histopathology as gold standard. Validation study Study was carried out at Rawalpindi Leprosy Hospital, Dermatology Department Military Hospital [MH] and Armed Forces Institute of Pathology [AFIP], Rawalpindi from 18[th] August 2012 to 18 Feb 2013. Appropriate technical and ethical approval for the study and patient consent were obtained. All suspected patients of leprosy of any age and either gender having typical hypo-aesthetic or anesthetic, erythematous or hypo-pigmented scaly skin lesions on any part of body were included in this study. All patients who have already received treatment for leprosy, patients with pure neural leprosy, patient not giving their consent for skin biopsy and patients with lepra reactions were excluded from this study. Forty eight patients fulfilling the inclusion criteria were included in the study. Sample size had been calculated by using WHO sample size calculator taking confidence level 95%, absolute precision required 14% and anticipated population proportion 40%. Non-probability consecutive sampling technique was used to collect sample. The results of the study revealed that out of 48 clinically suspected patients of leprosy skin biopsy confirmed the diagnosis in 34 patients [70.8%] and the slit skin smear had diagnostic accuracy of 68.75% with sensitivity 55.8% and specificity and positive predictive value of 100%. Study suggested that although slit skin smears are rapid and inexpensive method of diagnosis but their diagnostic accuracy is low

11.
JPAD-Journal of Pakistan Association of Dermatologists. 2015; 25 (4): 327-330
em Inglês | IMEMR | ID: emr-181153

RESUMO

Graham-Little-Piccardi-Lasseur syndrome [GLPLS] is a rare variant of lichen planopilaris comprising of a triad of multifocal cicatricial alopecia of scalp, non-cicatricial alopecia of axillae and pubic region and keratotic follicular papules over body. Its exact etiology is not known to date, but it primarily involves an immune mediated inflammation affecting hair follicles resulting in cicatricial alopecia. We report a case of 55 years old female diagnosed as having features of this syndrome with cicatricial alopecia of FFA and FADP.

12.
JPAD-Journal of Pakistan Association of Dermatologists. 2015; 25 (3): 182-185
em Inglês | IMEMR | ID: emr-173840

RESUMO

Objective: To determine frequency of undiagnosed diabetes mellitus in patients with herpes zoster. [HZ]


Methods: This cross-sectional study was performed at PNS Shifa hospital, Karachi from June, 2013 to December, 2013. A total of 89 patients suffering from HZ from age 40-70 years were included in this study after taking informed consent. All patients underwent fasting blood sugar evaluation from hospital laboratory


Results: 34 [38.2%] patients were of 40-55 years of age while 55 [61.8%] were of 56-70 year age group. Mean age was 56.93 +/- 8.24 years, 48 [53.9] were male and 41 [46.1%] were females while undiagnosed diabetes mellitus in patients with HZ occurred in 36 [40.5%] while 53 [59. 5%] had no findings of the morbidity


Conclusion: Frequency of undiagnosed diabetes mellitus is higher among patients with herpes zoster. So, it is recommended that every patient who present with HZ, should be evaluated for diabetes mellitus


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Idoso , Herpes Zoster , Estudos Transversais
13.
JPAD-Journal of Pakistan Association of Dermatologists. 2015; 25 (3): 216-219
em Inglês | IMEMR | ID: emr-173847

RESUMO

Bazex-Dupre-Christol syndrome [BDCS] is clinically characterized by multiple basal cell carcinomas of the face occurring mainly during the second and third decade of life, follicular atrophoderma predominantly of the dorsum of hands and feet and generalized hypotrichosis, sometimes with pili torti and trichorrhexis nodosa. Common associated features are milia, hypohidrosis and calcifying epithelial tumours. We herein report four members of one family with BDC syndrome, a mother and her three daughters. In the mother and one daughter, the clinical picture was very typical with all major features, whereas in the others only follicular atrophoderma, milia and hypotrichosis were present. BDCS is a hereditary multiple BCC syndrome whose pattern of inheritance is thought to be X-linked dominant, which implies that all daughters of the affected mothers should have this disease. In this case three out of four daughters are suffering from BDCS but one is totally asymptomatic. To our knowledge, this is the first report of a family with BDC from Pakistan


Assuntos
Humanos , Feminino , Pessoa de Meia-Idade , Neoplasias Cutâneas , Hipotricose
14.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2015; 25 (5): 324-327
em Inglês | IMEMR | ID: emr-166722

RESUMO

To compare the mean values of lipid profile in psoriatic patients and healthy controls. Case control study. Department of Dermatology, PNS Shifa, Karachi, from November 2012 to April 2013. Patients with psoriasis fulfilling the inclusion and exclusion criteria were selected from Dermatology Outpatient Department [OPD] of PNS Shifa, Karachi. After fasting for 14 hours, 5 ml of venous blood was drawn in sterile syringe and submitted to the Hospital Laboratory for lipid profile, by enzymatic method on Hitachi [Roshe[Registered sign]] using reagents by the same firm. The mean values lipid profile in psoriatic patients versus healthy controls were recorded and compared. A total of 256 patients [128 in each group] were enrolled. Mean lipid profile in both groups revealed cholesterol [mg/dl] value of 203.43 +/- 11.43 in cases and 173.64 +/- 13.65 in controls. Triglyceride [mg/dl] was 178.87 +/- 43.60 and in cases 144.23 +/- 34.01 in controls, HDL-C [mg/dl] was 37.81 +/- 10.78 in cases and 41.41 +/- 9.72 in controls while LDL-C [mg/dl] was 139.52 +/- 13.71 in cases and 109.44 +/- 13.80 in controls. Each parameters had p-value < 0.05 which was significant. Dyslipidemia was found in a high percentage of psoriatic patients than healthy controls. Psoriatic patients require thorough lipid and cardiovascular examinations as they should be considered as individuals with increased risk of cardiovascular diseases


Assuntos
Humanos , Masculino , Feminino , Estudos de Casos e Controles , Dislipidemias , Lipídeos/sangue
15.
PAFMJ-Pakistan Armed Forces Medical Journal. 2015; 65 (3): 367-370
em Inglês | IMEMR | ID: emr-165804

RESUMO

To measure in-vitro susceptibility of Sarcopties Scabieivar Hominis to 5% permethrin and 1% lindane.Study Design: Randomized controlled trials. Study was carried out at Dermatology Department, Military Hospital, Rawalpindi from January 2012 to June 2012. A total of 60 mites from 60 patients were taken for assay. Mites from every patient were randomly allocated to two groups i.e. group A [5% permethrin] and group B [1% lindane]. Permethrin and lindane were applied in a thin film over a glass slide. Live mites were then gently transferred to the glass slide and covered with a lid. Mites were inspected for leg movements at time interval of 1hr, 2hrs, 3hrs, 4hrs and 5hrs. Death was declared once all leg movements had ceased. All mites which died within 5 hours had been declared as susceptible to drugs, while mites having active leg movements even after 5 hours of drug application were considered as non-susceptible. A total of 93.33% [n=28] of mites in group-A died within 5 hours of application of permethrin [susceptible] and 6.67% [n=2] of mites in group-A were alive after 5 hours of drug application [resistant] While 53.33% [n=16] of mites in group-B died within 5 hours of application of lindane [susceptible] and 46.67% [n=14] of mites in group-B did not die after 5 hours [non-susceptible], [p value < 0.001]. Permethrin is more effective as compared to lindane against Sarcopties Scabei in terms of in-vitro susceptibility

16.
JPAD-Journal of Pakistan Association of Dermatologists. 2014; 24 (4): 355-357
em Inglês | IMEMR | ID: emr-162422

RESUMO

Herpes zoster is a common disease of the dorsal root ganglia and sensory nerve fibers, clinically characterized by unilateral painful vesicular eruption of the skin in a dermatomal distribution. Segmental motor weakness is a rare complication that occurs in 0-5 percent of patients and is associated with an excellent prognosis for recovery. We herein, present a case of herpes zoster complicated by segmental motor paresis of abdominal musculature resulting in pseudohernia. This rare complication of herpes zoster, with an excellent prognosis for recovery, should be recognized by dermatologists and surgeons as it can save costly consultations and evaluations

17.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2014; 24 (10): 763-765
em Inglês | IMEMR | ID: emr-149787

RESUMO

Kindler's Syndrome [KS] is a rare genodermatosis with autosomal recessive mode of inheritance. The disease results from homozygous mutations on both alleles of the FERMT-1 gene [also known as KIND-1 gene] that encodes the protein Kindlin-1 [kindlerin]. Clinical features include a constellation of early infantile skin blistering and mild photosensitivity, which improves with age, and progressive poikiloderma with widespread cutaneous atrophy. The differential diagnosis of Kindler syndrome include other congenital poikilodermatous and photosensitive conditions including Bloom syndrome, Cockayne syndrome, dyskeratosis congenita, epidermolysis bullosa, Rothmund-Thomson syndrome and xeroderma pigmentosum. We herein, report the presence of the Kindler's syndrome in 5 out of 7 children of consanguineous parents. To authors' knowledge, this is the first report of Kindler's syndrome involving 5 members of a family


Assuntos
Humanos , Masculino , Feminino , Epidermólise Bolhosa/diagnóstico , Doenças Periodontais/diagnóstico , Transtornos de Fotossensibilidade/diagnóstico , Consanguinidade , Criança , Família
18.
JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2012; 22 (12): 786-788
em Inglês | IMEMR | ID: emr-151990

RESUMO

The term Pseudoainhum is used in medical literature to elaborate the presence of constricting bands around the digits of hands and feet due to variety of etiologies. This phenomenon can lead to irreversible damage to the supplying neurovasculature and sequential autoamputation of the affected digits. The report herein, describes the rare presentation of pseudoainhum occurring concomitantly in acute psoriasis. Timely recognition of such rare disease entities by physicians is imperative to avoid unnecessary complications

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