AFP Journal Review: January 1, 2008 John W. Hariadi, M.D. Newborn Skin: Part I. Common Rashes Rashes extremely common in 1st 4 weeks of life Mostly benign and self-limited Transient Vascular phenomenon Erythema Toxicum Acne Neonatorum Milia, Miliaria Seborrheic Dermatitis Clinical Recommendation Evidence ratin g Infants who appear sick and have vesiculopustular rashes should be tested for Candida, viral, and bacterial infections. C Acne neonatorum usually resolves within four months without scarring. In severe cases, 2.5% benzoyl peroxide lotion can be used to hasten resolution. C Miliaria rubra (also known as heat rash) responds to avoidance of overheating, removal of excess clothing, cool baths, and air conditioning. C Infantile seborrheic dermatitis usually responds to conservative treatment, including petrolatum, soft brushes, and tar-containing shampoo. C Resistant seborrheic dermatitis can be treated with topical antifungals or mild corticosteroids. B A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evi = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information SORT evidence rating system Transient Vascular Phenomena Normal Newborn Physiology rather than true “rashes” Cutis Marmorata and Harlequin Color Change Cutis Marmorata Normal reticulated Mottling of skin Trunks and extremities Vascular response to cold May persist for weeks or months Generally resolves when skin is warmed Harlequin Color Change ?Caused by immaturity of hypothalamic center that controls dilation of peripheral blood vessels Occurs when newborn lies on side Erythema of dependent side with blanching of contralateral side Persists for 30 seconds to 20 minutes Resolves with crying or increased muscle activity Up to 10% of full term infants From 2nd-5th day of life, may continue up to 3 weeks Erythema Toxicum Neonatorum Most common pustular eruption in newborns (40-70%) Common in term infants and those >5.5 lbs Present at birth, 2nd-3rd DOL Erythematous 2-3 mm macules & papules pustules Pustule surrounded by blotchy area of erythema –”flea bitten” Face, trunk, proximal extremities-spares palms/soles Erythema Toxicum Neonatorum Generally clinical diagnosis Cytologic exam of pustuleeosinophilia with Gram, Wright, Giemsa Stain Etiology is unknown Fade over 5-7 days, may recur for several weeks No treatment needed If sick appearing, need to r/o infectious cause Table 1. Infectious Causes of Vesicles or Pustules in the Newborn Class Cause Distinguishing features Bacterial Group A or B Streptococcus Listeria monocytogenes Pseudomonas aeruginosa Staphylococcus aureus Other gram-negative organisms Other signs of sepsis usually present Elevated band count, positive blood culture; Gram stain of intralesional contents shows polymorphic neutrophils Fungal Candida Presents within 24 hours after birth if congenital, after one week if acquired during delivery Thrush is common Potassium hydroxide preparation of intralesional contents shows pseudohyphae and spores Spiroche tal Syphilis Rare Lesions on palms and soles Suspect if results of maternal rapid plasma reagin or venereal disease research laboratory test positive or unknown Viral Cytomegalovirus Herpes simplex Varicella zoster Crops of vesicles and pustules appear on erythematous base For herpes simplex and varicella zoster, Tzanck test of intralesional contents shows multinucleated giant cells Transient Neonatal Pustular Melanosis Vesiculopustular rash 5% Black, ,1% White Lesions lack surrounding erythema Pigmented macules within the vesiculopustules Rupture easilyleave behind scales & pigmented macules All areas affected including palms/soles Fade over 3-4 weeks Cytology: PMNs Acne Neonatorum 20% of newborns Closed comedones on forehead, nose, cheeks Open comedones, inflammatory papules Stimulation of sebaceous glands by maternal androgens Resolve within 4 months without scarring Treatment usually not required; can use 2.5% benzoyl peroxide Persistent/Severe need to look for underlying causes Milia 1-2 mm pearly white/yellow papules Retention of keratin within dermis Up to 50% of newborns Forehead, nose, cheeks, chin but can also: trunk, penis, limbs, mucous membranes Resolve within 1st month, can last till 2nd or 3rd month Miliaria Sweat retention by partial closure of eccrine structures 40% of infants-1st MOL Miliaria Crystallina – – Miliaria Rubra-”Heat Rash” – – 1-2mm vesicles without surrounding erythema Hours to days Erythematous papules, in covered portions of skin Deeper level of sweat gland obstruction Avoid overheating, remove excess clothing, cooling baths, air conditioning Seborrheic Dermatitis Extremely common “Cradle Cap”-may include face, ears, neck Erythema in flexural folds, scaling on scalp Often involves diaper area Can be difficult to distinguish from atopic dermatitis Table 2. Distinguishing Features of Seborrheic and Atopic Dermatitis in Infancy Feature Seborrheic dermatitis Atopic dermatitis Age at onse t Usually within first month After three months of age Course Self-limited, responds to treatment Responds to treatment, but frequently relapses Distributi Scalp, face, ears, neck, on diaper area Scalp, face, trunk, extremities, diaper area Pruritus Ubiquitous Uncommon Seborrheic Dermatitis Etiology unknown-? Malassezia furfur, hormonal fluctuations Self limited- resolves several weeks to months Conservative approach – – – Watchful waiting Soft Brush after shampooing Emollient Table 3. Treatment Options for Infantile Seborrheic Dermatitis Medication Directions Cost (generic)* White petrolatum Apply daily $3 for 30 g May soften scales, facilitating removal with soft brush Tar-containing shampoo Use several times per week $13 to $15 for 240 mL Use when baby shampoo has failed Safe, but potentially irritating Ketoconazole (Nizoral, brand no longer available in the United States), 2% cream or 2% shampoo Cream: apply to scalp three times weekly Shampoo: lather, leave on for three minutes, then rinse. Use three times weekly Cream: ($16 to $37 for 15 g) Shampoo: $30 to $33 for 120 mL ($16 to $38) Small trial showed no systemic drug levels or change in liver function after one month of use Hydrocortisone 1% cream Apply every other day or daily $2 to $4 for 30 g Limit surface area to reduce risk of systemic absorption and adrenal suppression May be especially effective for rash in flexural areas Notes Newborn Skin: Part II Birthmarks 3 Main groups – Pigmented – Vascular – Congenital melanocytic Nevi Dermal Melanosis Hemangiomas Nevus Flammeus, Nevus Simplex Abnormal development Most do not require immediate treatment Clinical recommendation Patients with large congenital melanocytic nevi should be referred to a surgeon and followed for recurrence. Evidence C Uncomplicated hemangiomas that are not near the eyes, lips, nose, or perineum do not require treatment. C Infants with port-wine stains near the eyes should be referred for glaucoma testing. C Patients with multiple midline lumbosacral skin lesions or a C single high-risk lesion should undergo magnetic resonance imaging or ultrasonography to rule out occult spinal dysraphism. Congenital Melanocytic Nevi 0.2-0.4% infants at birth Disrupted migration of melanocytic precursors in neural crest Color: Brown to black Mostly flat, can be raised Potential for malignancybased on size Nevus that changes in color, shape or thickness need further evaluation Table 1. Management of Congenital Melanocytic Nevi by Size Size Projected size in Size during infancy adulthood Management strategy Giant >14 cm > 40 cm Remove nevus, observe for recurrence in original or distal sites Large > 7 cm on torso, buttocks or extremities; >12 cm on head 20 to 40 cm Remove nevus, observe for recurrence in original or distal sites Medium 0.5 to 7 cm 1.5 to 20 cm Consider referral to dermatologist for observation Small < 0.5 cm < 1.5 cm Observe in primary care setting Dermal Melanosis “Mongolian Spots” Flat, most often in back or buttocks Arise when melanocytes trapped deep in the skin Common in Non-white populations Should be documented in newborn exam Most fade by 2 years of age Hemangiomas 1.1-2.6% of newborns Can develop anytime in 1st few months of life, 10% at 1 year 50% involute by 5 years, 70% by 7 years and 90% by age 10 May leave scars Can treat with pulse dye laser—unsure long term cosmetic outcome Eye, airway or organ compression require immediate treatment & referral – Prednisone 3mg/kg x 6-12 weeks Nevus Flammeus “Port Wine Stain” 0.3% of newborns Flat,dark red to purple lesions Do not fade over time May develop varicosities, granulomas, nodules Do not require treatment—Pulse dye laser before age1 Opthalmic (V1) distribution associated with glaucoma – 5-8% with Sturge-Weber Syndrome – glaucoma/seizures/port-wine stain, angioma of brain/meninges Mental retardation & hemiplegia Refer to Ophthalmology Nevus Simplex “Stork bites” ,“Angel Kisses” , “Salmon patch” Flat, salmon colored lesions-telengectasias in dermis Eyes, scalp, neck—blanch when compressed Occur on both sides of face in symmetric pattern 40% resolve in neonatal period, most by 18 months Supernumerary Nipples Arise from mammary ridges along ventral body wall May contain areola, nipple or both May be unilateral/bilateral Up to 5.6% of children Mostly benign Skin Markers of Spinal Dysraphism Spinal dysraphism: – – diverse congenital spinal anomalies caused by incomplete fusion of midline elements of the spine Tethered Cord Syndrome-need surgical release Midline lumbosacral skin lesions are often cutaneous markers of spinal dysraphism – – High or intermediate risk lesions should undergo imaging MRI is most sensitive. Spinal ultrasonography also used Table 2. Cutaneous Markers and Risk of Occult Spinal Dysraphism Risk of occult spinal dysraphism Suggested evaluation Any one of the following: Dermal sinus Lipoma Tail High MRI Any one of the following: Aplasia cutis congenita Atypical dimple Deviation of gluteal furrow Intermediate MRI or ultrasonography Any one of the following: Hemangioma Hypertrichosis Mongolian spot Nevus simplex Port-wine stain Simple dimple Low No evaluation needed in most cases; may consider ultrasonography depending on local standard of care Two or more lesions of any type High MRI Skin lesion Clavicle Fractures 5-10% of all fractures Most in men<25 yrs, men >55 & women >75 Allman Classification – – – Group I (midshaft/middle third) ->75-80%, young Group II (lateral/distal)-> 15-25% Group III (medial/proximal)-> 5% Clinical recommendation Nonoperative treatment is preferred for nearly all acute, nondisplaced midshaft clavicle fractures. Evide nc e B Treatment with an arm sling is preferred over a figure-of-eight dressing for B acute midshaft clavicle fractures because it is better tolerated and leads to similar outcomes. Displaced midshaft clavicle fractures may be managed nonoperatively, but plate fixation should be considered. B Nonoperative treatment is preferred for distal clavicle fractures because outcomes are the same whether or not bony union is achieved. B Anatomy Midshaft is thinnest, least medullous area AC & SC joints have robust ligamentous support Sternal ossification center fuses with shaft by age 30 Malunion can impair mobility to upper extremity Callus formation/ displacement can lead to thoracic outlet obstruction Evaluation Mechanism of injury: fall directly on shoulder with arm at side, often in contact sports Hold affected arm adducted close, support with opposite hand Exam: ecchymosis, edema,focal tenderness and crepitus on palpation of clavicle Need to perform neurovascular & lung exam Radiographs should be performed Midshaft Clavicle Fractures Midshaft Clavicle Fractures Nondisplaced – – – Sling /Figure of eight dressing Can discontinue in 1-2 weeks when pain subsides Pendulum exercises as soon as pain allows, active ROM & strengthening 4-8 weeks Displaced – – Higher rates of nonunion Can consider operative treatment in patients with multiple risk factors Table 1. Risk Factors for Nonunion of Midshaft Clavicle Fractures Clavicle shortening > 15-20 mm Female sex Fracture comminution Fracture displacement Greater extent of initial trauma Older age Midshaft Clavicle Fractures Operative options: – – Open/closed reduction with plate fixation Intramedullary fixation->smaller incisions, avoids plate pressure but risk of device migration Complications rare->pneumothorax, vascular injury Long term Sequelae: Pain, weakness, parasthesias Displacement of > one bone width is strongest radiographic risk factor for symptoms & sequealea Return To Activity Considerations Full Range of motion Normal shoulder strength Clinical & radiographic evidence of bone healing No tenderness Can return to noncontact sports in 6 weeks Contact sports in 2-4 months If surgical case->may need removal of hardware Midshaft Clavicle Fractures in Children 88 percent of clavicle fractures Nearly all heal well due to great periosteal regenerative potential Often have significant callus formation Healing within 4-6 weeks If no history of trauma, need to consider malignancy, rickets, osteogenesis imperfecta and physical abuse Distal Clavicle Fractures 5 Types: – – – – – Type I Coracoclavicular ligament intact Type II Conoid (medial) torn, trapezoid intact Type III Extension into AC joint Type IV Disruption in periosteal sleeve (children) Type V Avulsion of ligaments with small cortical fragment Type I & III-stable nonoperative Type II->high rate of nonunion Type IV-often occurs through distal physis with ligaments attached-> “pseudodislocation” – Operative treatment only with sever displacement Proximal Clavicle Fractures Very uncommon Typically nondisplaced If displaced, need to evaluate for neurovascular compromise May need CT scan for better visualization Herbal and Dietary Supplement-Drug Interactions in Patients with Chronic Diseases Herbs, Vitamins and supplements may augment or antagonize actions of drugs Deleterious effects are most pronounced with anticoagulants, cardiovascular medications, oral hypoglycemics and antiretrovirals St. John’s Wort – Reduction in INR with warfarin, reduced levels of verapamil, statins, digoxin, antiretrovirals Physicians should routinely ask patients about use of supplements
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