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2.
Article in English | MEDLINE | ID: mdl-18595198

ABSTRACT

BACKGROUND: Acne neonatorum (AN) is characterized by a facial eruption of inflammatory and noninflammatory acne lesions in a neonate. Hyperactivity of sebaceous glands, stimulated by neonatal androgens, is implicated in its pathogenesis. AIM: To elucidate the clinical profile of AN in eastern Saudi Arabia. METHODS: All patients diagnosed with AN in King Fahd Hospital of the University in Khobar, Saudi Arabia, during the year 2005 were evaluated clinically. RESULTS: AN was diagnosed in 26 patients (male/female ratio 1:1). The lesions included mainly facial comedones (30.8%); papules and pustules (15.3% each); and combination of papules, pustules, and cysts (53.4%). CONCLUSION: All patients recovered spontaneously. In 50% of the cases, one of the parents reported having had acne vulgaris during adolescence. Hereditary factors seem to play a significant role in our series.


Subject(s)
Acne Vulgaris/pathology , Skin/pathology , Face/pathology , Female , Humans , Infant, Newborn , Male , Pregnancy , Prospective Studies , Risk Factors , Saudi Arabia , Surveys and Questionnaires
3.
J Drugs Dermatol ; 7(5): 457-62, 2008 May.
Article in English | MEDLINE | ID: mdl-18505138

ABSTRACT

BACKGROUND: Herpes zoster (HZ), caused by varicella zoster virus (VZV), initially produces chicken-pox, then the virus lies dormant in the dorsal root ganglia. The virus can reactivate after many years and results in HZ along ganglion's distribution. Old age, trauma, stress, diabetes mellitus, and immune suppression are important risk factors for the reactivation. Herpes zoster is characterized by unilateral radicular pain and vesicular eruption that is generally limited to the dermatome innervated by the affected ganglion. In immunocompromised individuals, disseminated zoster may develop. The aims of therapy in HZ are to control pain or reduce its severity by the use of analgesics, reduce the duration and eruption of new lesions, and prevent complications, particularly postherpetic neuralgia (PHN) by appropriate antiviral therapy. METHODS: All cases of HZ seen in the dermatology clinic at King Fahd Hospital of the University (KFHU) from 1988 to 2006 were included in the study. Their diagnoses were based on the clinical presentation. The following parameters were collected and analyzed: age, sex, nationality, symptoms, dermatomal distribution, complications, coexisting diseases, and disease management. RESULTS: Of 22 749 new cases seen in the dermatology clinic over 18 years, 141 were HZ, with an occurrence of 0.62%. Male to female ratio was 2:1 and the age ranged from 14 months to 80 years. The thoracic dermatomes were the most commonly involved. The most frequent coexisting disease was diabetes mellitus, and the most common complication of HZ was PHN. Most patients with HZ ophthalmicus developed eye complications. CONCLUSION: The occurrence of HZ is 0.62% in patients reporting to the dermatology clinic of the hospital. Males are little more affected than females. The thoracic dermatomes are the most frequently involved. Diabetes mellitus is the most frequent coexisting disease. Postherpetic neuralgia is the most common complication of HZ.


Subject(s)
Herpes Zoster/diagnosis , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Herpes Zoster/complications , Herpes Zoster/drug therapy , Humans , Infant , Male , Middle Aged , Neuralgia, Postherpetic/drug therapy
4.
Int J Dermatol ; 45(3): 257-64, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16533225

ABSTRACT

BACKGROUND: A total of 10 455 new dermatology patients were seen in the dermatology clinics of King Fahad Hospital of the University (KFHU), Al-Khobar, Saudi Arabia, between January 1990 and December 1995. We identified 71 patients with a histopathologically confirmed diagnosis of specific forms of primary hereditary ichthyoses (PHI). We have reviewed the epidemiological and clinical features of these patients. OBJECTIVE: To document the epidemiological and clinical features of patients with PHI in the Eastern Province of Saudi Arabia. METHODS: We used the dermatology out-patient department (OPD) logbooks to identify cases of PHI from new patients presenting with different dermatological problems over a 6-year period. We used specifically designed protocol forms to extract epidemiological and clinical data from the study patients' medical records. These were entered into a computer database and analyzed using standard statistical software. RESULTS: A total of 71 patients, 44 males and 27 females (male : female sex ratio of 1.63 : 1), were identified from a total of 10 455 new patients seen in our dermatology clinics between January 1990 and December 1995. The occurrence rate of PHI, in our clinics, was 0.67% or 7 per 1000 new dermatology cases. The clinical pattern of PHI showed that Icthyosis Vulgaris was the most common form seen, followed by Nonbullous Ichthyosiform Erythroderma. Thirty-one patients (44.7%) with Ichthyosis Vulgaris (IV) were seen: 12 patients (16.9%) with X-linked Recessive Ichthyosis (XLRI), four patients (5.6%) with Lamellar Ichthyosis (LI), three patients (4.2%) with Bullous Ichthyosiform Erythroderma (BIE) and 21 patients (29.6%) with Nonbullous Ichthyosiform Erythroderma (NBIE). There was a significantly high consanguinity rate in our patients (85%), and the family history was positive in 53 cases out of the 71 (75%). CONCLUSIONS: This preliminary study is the first report of its kind from Saudi Arabia and documents the clinico-epidemiological features of PHI patients in the Eastern Province. The high rate of parental consanguinity among our Saudi patients may account for the high proportion of patients with a positive family history. Consanguinity also probably explains why the most severe forms of PHI were seen in a significant number of new patients' siblings. These severe forms of PHI (Nonbullous Ichthyosiform Erythroderma, Bullous Ichthyosiform Erythroderma and Lamellar Ichthyosis) together constituted nearly 40% of all cases.


Subject(s)
Consanguinity , Genetic Diseases, Inborn/epidemiology , Ichthyosis/epidemiology , Age of Onset , Female , Genetic Predisposition to Disease , Health Surveys , Humans , Incidence , Infant , Infant, Newborn , Male , Retrospective Studies , Saudi Arabia/epidemiology
5.
Saudi Med J ; 26(10): 1607-10, 2005 Oct.
Article in English | MEDLINE | ID: mdl-16228065

ABSTRACT

OBJECTIVES: To describe the pattern of skin disease in the Eastern Province and compare it with similar studies carried out in other regions of Saudi Arabia. METHODS: All new dermatology cases reporting at King Fahd Hospital of the University in Al-Khobar, Saudi Arabia, seen between August 2002 to July 2003 were reviewed. RESULTS: One thousand and seventy-six new patients within the period of the study were seen. Dermatitis/ eczema was the most frequent dermatosis (19.6%) with atopic dermatitis forming 35.9% among eczemas, followed by acne (13.8%), viral infection (13.5%), of which 11.9% had viral warts; pigmentary disorders (9.7%) with vitiligo comprising 5% of the total. In fungal infections (9.6%), dermatophytoses formed 6.3% of the total patients, alopecias 7.2%, papulosquamous disorders 6.4%, of which 3.4% had psoriasis and 1.7% had lichen planus; urticaria 5.7%, pyoderma 4.8%, and the parasitic infections, 1%. CONCLUSION: This comparative study showed that eczema was the most frequent diagnosis among all skin diseases and parasitic infections were the least frequent diseases. Generally, the Eastern Province study is closely comparable to other studies in the country with higher frequencies of viral and fungal infections and acne.


Subject(s)
Skin Diseases/diagnosis , Skin Diseases/epidemiology , Adolescent , Adult , Age Distribution , Aged , Child , Child, Preschool , Cross-Sectional Studies , Developing Countries , Female , Humans , Incidence , Male , Middle Aged , Prognosis , Saudi Arabia/epidemiology , Severity of Illness Index , Sex Distribution
6.
Int J Dermatol ; 43(6): 415-9, 2004 Jun.
Article in English | MEDLINE | ID: mdl-15186221

ABSTRACT

BACKGROUND: Of 10,455 new dermatology patients seen at the Dermatology Clinic of King Fahad Hospital of the University, Al-Khobar, Saudi Arabia, between January 1990 and December 1995, the epidemiologic and demographic features of 71 patients, each with a histopathologically confirmed diagnosis of one specific type of primary hereditary ichthyosis (PHI), have been reviewed. OBJECTIVE: To study and document the epidemiologic and demographic profiles of patients with PHI in the Eastern Province of Saudi Arabia. METHODS: From the outpatient department dermatology logbooks, 71 patients with PHI, from 10,455 new cases with different dermatologic problems seen during the 5-year period, were included in this study. Using specially designed protocol forms, epidemiologic and demographic data were extracted from the medical records of the patients, entered into a computer, and analyzed using the SPSS program. RESULTS: Seventy-one patients with PHI, 44 males and 27 females (ratio, 1.63 : 1), were seen at our Dermatology Clinic between January 1990 and December 1995. The occurrence rate of PHI in our clinic is 0.67%, i.e. approximately 7 per 1000 new cases. The clinical pattern of PHI was as follows: 31 patients (44.7%) with ichthyosis vulgaris (IV), 12 (16.9%) with X-linked recessive ichthyosis (XLRI), four (5.6%) with lamellar ichthyosis (LI), three (4.2%) with bullous ichthyosiform erythroderma (BIE), and 21 (29.6%) with nonbullous ichthyosiform erythroderma (NBIE). IV was most common, followed by NBIE. Parental consanguinity was high (approximately 85%), and the family history was positive in 53 of the 71 cases (75%). CONCLUSIONS: This preliminary study has attempted to document the epidemiologic patterns of PHI patients in Saudi Arabia and, to our knowledge, this is the first report of its kind in this country. We found a high rate of parental consanguinity, a high percentage of patients with a positive family history, and many siblings affected by the severest forms of PHI, namely NBIE, BIE, and LI, which accounted for 39.4% of all cases of PHI.


Subject(s)
Ichthyosis/epidemiology , Adolescent , Adult , Aged , Child , Child, Preschool , Consanguinity , Female , Genetic Predisposition to Disease , Humans , Ichthyosis/etiology , Ichthyosis/genetics , Infant , Infant, Newborn , Male , Medical Records , Middle Aged , Pedigree , Retrospective Studies , Saudi Arabia/epidemiology
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