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Neonatal Abdominal Masses
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Neonates 75-80% Most common Bulky and smooth Flank
Benign genitourinary lesions Most common Congenital obstructive hydronephrosis Multicystic dysplastic kidney Bulky and smooth Flank Flank mass due to UPJ obstuction leading to hydronephrosisi
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Neonates GU masses Ureteral duplications and Ureteroceles PUV
May produce obstructive uropathies that lead to palpable masses PUV Bilateral flank masses Most common cause of distal urinary tract obstruction in boys
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Neonates Mulitcystic dysplastic kidney Renal vein thrombosis
Unilateral, soft, cystic Renal vein thrombosis Hyperviscocity syndromes Severe neonatal dehydration Mesoblastic nephroma Benign renal tumor Mimics Wilms
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Neonates Ovarian cysts Congenital vaginal obstruction
Maternal hormone stimulation Withdrawal leads to resolution >5cm at risk for torsion Should be aspirated Congenital vaginal obstruction GI duplication cysts Diagnosis often made later
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Neonates Mesenteric and omental cysts Soft, diffuse and multiloculated
Due to congenital lymphatic obstruction May have acute hemorrhage Acute abdominal pain
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Neonates Adrenal masses Common Benign Malignant
Spontaneous adrenal hemorrhage Perinatal stress Birth trauma Neuroblastoma Malignant Left suprarenal heterogeneous mass suspicious for neuroblastoma
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Neonates Intra-abdominal extra lobar sequestration
Adjacent to adrenal gland Suggests a malignancy Sacrococcygeal teratoma Most common malignancy of infancy
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Toddlers and young children
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Hepatic Lesions Bulky RUQ mass Fixed Benign Hemangioendothelioma AVM
Mesenchymal hamartoma Choledochal cysts
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Splenic Lesions Underlying hematologic disease Splenic cysts
Immunodeficiency Lymphoproliferation Splenic cysts Congenital Trauma
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Older children and teens
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Question 7 A premenstral 12 yo F presents to clinic with a history of abdominal pain occuring once a month. The abnormal physical exam finding is pictured. What other abnormalities is this patient at risk for? A. GU B. Cardiac C. Brain D. GI E. Limb Answer A
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Ovarian Masses Mostly seen in adolescence >75% benign 25% Cystic
Solid Malignant changes
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Vaginal Obstruction Puberty Newborns Cyclic abdominal pain
Large pelvic or lower abdominal mass Absence of menses May have hydronephrosis Obstruction Coexisting GU abnormalities Newborns Hydrocolpos
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Inflammatory masses
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Inflammatory Masses Characteristics Causes
Tender Systemic symptoms Persistent signs of sepsis Causes Bowel perforations Meckel diverticulitis Crohns VP shunts Omentum and adjacent bowel loops migrate to localize the process and an abscess cavity forms
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Inflammatory Masses Treatment Crohns IV antibiotics
Percutaneous drainage Crohns Fistula Failure to respond to medical therapy Upper GI with SBFT BE
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Head and neck masses
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Head and Neck Most lesions are benign Critical PE findings
Determination of size Evidence of airway compromise Signs of inflammation Presence of sinus tracts Ocular involvement
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Head and Neck Radiology Endoscopic procedures CT or MRI
Bony structures Vascular structures Brain involvement Endoscopic procedures Nasopharyngoscopy, laryngoscopy and esophagoscopy Disorders of breathing, swallowing or phonation
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Head and Neck Surgery Frequently necessary for diagnosis and therapy
Unnecessary cases Hemangioma Torticollis Benign reactive adenopathy
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Scalp
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Question 8 The parents of a 1 month old M infant are concerned about a red lesion that has appeared on his upper forehead. On exam, it appears to be a small 1cm hemangioma. What do you tell them? A. This child needs referral to a dermatologist for medical treatment B. The lesion is benign and will resolve during the first 7 years of life C. Surgical intervention is necessary because it is on the face D. The lesion is unlikely to resolve on its own E. This lesion has a high malignant potential Answer B
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Scalp Hemangiomas Benign, congenital vascular tumors
Most frequent in head and neck Characteristics Raised Red or purple May blanch May not be present at birth Develop in the first few months of life
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Scalp Hemangiomas Kasabach-Merritt Syndrome Typical course
Due to rapid growth and expansion Platelet sequestration Coagulopathy Refractory to treatment Typical course Benign Spontaneous resolution over first 7 years Surgical intervention Airway compromise Periorbital involvement
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Dermoid Cysts Congenital lesions Composed of
Hair Skin Sebaceous structures Occur in areas of embryonic fusion Most frequent in head and neck Also found in sacral, perineal and sternal region
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Dermoid Cysts Characteristics
Well-circumscribed Firm Fixed to deep structures Always evaluate by MRI before surgical intervention for extention Treatment is surgical
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FACE
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Face Preauricular skin tags Preauricular pits or sinuses
Vestigial cartilaginous remnants Cosmetic Preauricular pits or sinuses Prone to infectious complications Epidermal inclusion structures Most lesions asymptomatic Surgical resections for infectious complications
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Face Parotid Gland Hemangiomas Viral Bacterial Mycobacterial
Mumps Bacterial Staphylococcal Mycobacterial Atypicals or TB Chronic inflammatory conditions
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Face Intraoral lesions Ankyloglossia inferior Tongue-tie
Usually resolves spontaneously Regresses with feeding Speech problems if persistent Treatment Simple division
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Face Ranula Pseudocysts in the floor of the mouth
May spontaneously resolve Few become large Impairs lingual mobility Impairs speech Impairs breathing Treatment Marsupialization or complete excision
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Face Lymphangiomas May cause obstruction if mouth involved
Smaller, vesicular lesions located on the tongue may exude fluid that becomes purulent May need antibiotics Treatment Possible partial glossectomy Speech development, mandibular growth
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Face Lingual thyroid Rare developmental anomaly of the thyroid
Failure of thyroid descent Located at the base of the tongue (foramen cecum) Presentation Acute airway obstruction Lump in the throat on swallowing Hypothyroidism Treatment Thyroid replacement Surgical excision if obstructive
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