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2.
Clin Cosmet Investig Dermatol ; 10: 117-132, 2017.
Article in English | MEDLINE | ID: mdl-28458571

ABSTRACT

Dermatological disease can be devastating for patients, and although dermatologists are focused on remedying the cutaneous manifestations of these conditions, it is easy to miss the psychological suffering lurking below. Studies reveal that psychiatric comorbidity in dermatology is highly prevalent. Undetected psychopathology can greatly decrease a patient's quality of life and even contribute significantly to the clinical severity of their skin disease. For these reasons, it is vital that practitioners learn to detect psychological distress when it is present, and it is equally essential that they understand the treatment options available for effective intervention. Without training in psychiatric diagnosis and psychopharmacology, dermatologists can easily feel overwhelmed or out of their comfort zone when faced with the need to manage such conditions, but with the negative stigma associated with psychiatric disease in general, a psychiatric referral is often refused by patients, and the dermatologist is thus left with the responsibility. Uncertainty abounds in such situations, but this review seeks to alleviate the discomfort with psychodermatological disease and share practical and impactful recommendations to assist in diagnosis and treatment. In a busy dermatology clinic, the key is effective and efficient screening, combined with a repertoire of pharmacological and non-pharmacological treatment options that can be dispersed through an algorithmic approach according to the specific findings of that screening. By implementing these recommendations into practice, dermatologists may begin to gain comfort with the management of psychocutaneous disease and, as a specialty, may expand to fill a hole in patient care that is truly significant for patients, their families, and our communities as a whole.

4.
Dermatol Online J ; 22(3)2016 Mar 16.
Article in English | MEDLINE | ID: mdl-27136626

ABSTRACT

Pediculosis humanus capitus infestations are common and classically present with intense pruritus of the scalp. Although many treatment options are available, lice are becoming more resistant to conventional therapies and severe clinical presentations are bound to become more prevalent. We present a case of treatment-resistant pediculosis capitus resulting in diffuse autoeczematization of the torso and extremities and severe crusting and scaling of the scalp, which we called "crusted lice." This eruption differs from the well-described id reaction known as "pediculid" and represents a more dramatic manifestation of rampant infestation. This paper provides an up-to-date review of treatment options available for pediculosis humanus capitus, including newer medications like the ones that eventually led to resolution of our patient's extreme infestation.


Subject(s)
Coinfection/diagnosis , Eczema/diagnosis , Facial Dermatoses/diagnosis , Lice Infestations/diagnosis , Scalp Dermatoses/diagnosis , Staphylococcal Skin Infections/diagnosis , Animals , Anti-Bacterial Agents/therapeutic use , Coinfection/complications , Coinfection/drug therapy , Doxycycline/therapeutic use , Drug Combinations , Eczema/complications , Eczema/drug therapy , Facial Dermatoses/complications , Facial Dermatoses/drug therapy , Female , Humans , Insecticides/therapeutic use , Ivermectin/therapeutic use , Lice Infestations/complications , Lice Infestations/drug therapy , Macrolides/therapeutic use , Middle Aged , Pediculus , Scalp Dermatoses/complications , Scalp Dermatoses/drug therapy , Severity of Illness Index , Staphylococcal Skin Infections/complications , Staphylococcal Skin Infections/drug therapy , Staphylococcus aureus , Torso
5.
Dermatol Res Pract ; 2015: 409637, 2015.
Article in English | MEDLINE | ID: mdl-26550011

ABSTRACT

Psoriasis is a chronic, immune-mediated skin condition with a high rate of psychiatric comorbidity, which often goes unrecognized. Beyond the negative consequences of mood disorders like depression and anxiety on patient quality of life, evidence suggests that these conditions can worsen the severity of psoriatic disease. The mechanisms behind this relationship are not entirely understood, but inflammation seems to be a key feature linking psoriasis with mood disorders, and physiologic modulators of this inflammation, including the hypothalamic-pituitary-adrenal axis and sympathetic nervous system, demonstrate changes with psychopathology that may be contributory. Cyclical disruptions in the secretion of the sleep hormone, melatonin, are also observed in both depression and psoriasis, and with well-recognized anti-inflammatory and antioxidant activity, this aberration may represent a shared contributor to both conditions as well as common comorbidities like diabetes and cardiovascular disease. While understanding the complexities of the biological mechanisms at play will be key in optimizing the management of patients with comorbid psoriasis and depression/anxiety, one thing is certain: recognition of psychiatric comorbidity is an imperative first step in effectively treating these patients as a whole. Evidence that improvement in mood decreases psoriasis severity underscores how psychological awareness can be critical to clinicians in their practice.

6.
Am J Med Genet A ; 167A(10): 2459-62, 2015 Oct.
Article in English | MEDLINE | ID: mdl-26059211

ABSTRACT

Terminal osseous dysplasia with pigmentary defects (TODPD) is a rare, X-linked syndrome classically characterized by distal limb anomalies, pigmented skin defects of the face, and recurrent digital fibromas. X-inactivation plays a major role in determining the range of phenotypic expression. Thus, patients can demonstrate a wide spectrum of disease severity, making accurate diagnosis more challenging. Recent studies have identified a FLNA c.5217G>A mutation as the cause of TODPD, allowing for diagnostic genetic testing. We present a case of molecularly confirmed TODPD in a girl with the 47,XXX chromosomal complement and deformities of the hands and feet, craniofacial abnormalities, and discolored, linear facial lesions. Skin biopsy of the patient's facial lesion revealed absent papillary dermal elastic fibers, consistent with anetoderma, which contrasts with the dermal hypoplasia described in the only other such facial biopsy reported in the literature. The finding of absent elastic fibers in the skin lesions suggests that mutated filamin A, in part, exerts its effects through dysregulated elastin biology, which may explain the nature of many connective tissue pleotropic effects in FLNA-related disorders.


Subject(s)
Anetoderma/genetics , Fibroma, Ossifying/genetics , Filamins/genetics , Fingers/abnormalities , Genetic Diseases, X-Linked/genetics , Limb Deformities, Congenital/genetics , Mutation , Osteochondrodysplasias/genetics , Pigmentation Disorders/genetics , Toes/abnormalities , Anetoderma/complications , Anetoderma/diagnosis , Anetoderma/pathology , Female , Fibroma, Ossifying/complications , Fibroma, Ossifying/diagnosis , Fibroma, Ossifying/pathology , Fingers/pathology , Gene Expression , Genetic Diseases, X-Linked/complications , Genetic Diseases, X-Linked/diagnosis , Genetic Diseases, X-Linked/pathology , Humans , Infant, Newborn , Karyotype , Limb Deformities, Congenital/complications , Limb Deformities, Congenital/diagnosis , Limb Deformities, Congenital/pathology , Osteochondrodysplasias/complications , Osteochondrodysplasias/diagnosis , Osteochondrodysplasias/pathology , Pigmentation Disorders/complications , Pigmentation Disorders/diagnosis , Pigmentation Disorders/pathology , Toes/pathology , X Chromosome Inactivation
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