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Marilyn G. Liang, MD
Co-Director, Vascular Anomalies Center; Dermatologist, Dermatology Program; John B. Mulliken Chair in Vascular Anomalies
Associate Professor of Dermatology, Harvard Medical School
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Marilyn G. Liang, MD
Co-Director, Vascular Anomalies Center; Dermatologist, Dermatology Program; John B. Mulliken Chair in Vascular Anomalies
Associate Professor of Dermatology, Harvard Medical School
Medical Services
Languages
English
Education
Undergraduate School
Massachusetts Institute of Technology
1990
Cambridge
MA
Medical School
University of Rochester School of Medicine
1994
Rochester
NY
Internship
Strong Memorial Hospital
1995
Rochester
NY
Residency
Pediatrics
Strong Memorial Hospital
1996
Rochester
NY
Residency
Chief Resident (1998-1999)
Mayo Clinic Foundation
1999
Rochester
MN
Certifications
American Board of Dermatology (General)
American Board of Dermatology (Pediatric Dermatology)
Publications
Systemic and skin-limited delayed-type drug hypersensitivity reactions associate with distinct resident and recruited T cell subsets. View Abstract
Stigmatization and Mental Health Impact of Chronic Pediatric Skin Disorders. View Abstract
ACR Appropriateness Criteria® Soft Tissue Vascular Anomalies: Vascular Malformations and Infantile Vascular Tumors (Non-CNS)-Child. View Abstract
Immunohistochemical Expression of Lymphatic Endothelial Markers in Blue Rubber Bleb Nevus Syndrome. View Abstract
Multicenter Study of Long-Term Outcomes and Quality of Life in PHACE Syndrome after Age 10. View Abstract
Infantile Hemangioma of the Breast: Long-Term Assessment of Outcomes. View Abstract
Spectrum of lymphatic anomalies in patients with RASA1-related CM-AVM. View Abstract
Non-vascular intracranial lesions in three children with PHACE association. View Abstract
Next generation sequencing aids diagnosis and management in a case of encephalocraniocutaneous lipomatosis. View Abstract
Paradoxical Psoriasiform Eruptions in Children Receiving Tumor Necrosis Factor a Inhibitors. View Abstract
Metopic ridge presenting to pediatric dermatology and vascular anomalies clinics. View Abstract
Genomic analysis reveals germline and somatic PDGFRB variants with clinical implications in familial infantile myofibromatosis. View Abstract
Paraneoplastic pemphigus associated with Castleman disease: A multicenter case series. View Abstract
Topical treatment of pyogenic granulomas in a pediatric population: A single-institution retrospective review. View Abstract
Kaposiform Lymphangiomatosis: Pathologic Aspects in 43 Patients. View Abstract
Verrucous Venous Malformation-Subcutaneous Variant. View Abstract
Association of Demographic Factors and Infantile Hemangioma Characteristics With Risk of PHACE Syndrome. View Abstract
Mucocutaneous Adverse Events Associated With Oral Sirolimus for the Treatment of Vascular Anomalies. View Abstract
Classification of lower extremity venous malformations and risk of knee involvement: A retrospective cohort study. View Abstract
Early Features of Progressive Hemifacial Atrophy-Clinical and Imaging Findings. View Abstract
Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder. View Abstract
Pediatric facial pyoderma gangrenosum preceding the diagnosis of inflammatory bowel disease. View Abstract
Cutaneous manifestations of congenital malignant rhabdoid tumor: Unusual papillomatous plaques and other skin presentations. View Abstract
Diffuse capillary malformation with overgrowth contains somatic PIK3CA variants. View Abstract
Clinical and radiological characteristics of patients with retroperitoneal infantile hemangiomas. View Abstract
Pediatric leukemia cutis: A case series. View Abstract
Herpes zoster at the vaccination site in immunized healthy children. View Abstract
Holmes heart and tetralogy of Fallot in association with PHACE. View Abstract
Internal venous anomalies in patients with a genital venous malformation. View Abstract
A cross-sectional survey of long-term outcomes for patients with diffuse capillary malformation with overgrowth. View Abstract
Self-limited neonatal periumbilical erythema. View Abstract
Role of imaging in the diagnosis of parotid infantile hemangiomas. View Abstract
Wilms tumor screening in diffuse capillary malformation with overgrowth and macrocephaly-capillary malformation: A retrospective study. View Abstract
Sonographic screening for Wilms tumor in children with CLOVES syndrome. View Abstract
A somatic GNA11 mutation is associated with extremity capillary malformation and overgrowth. View Abstract
PHACE Syndrome: Consensus-Derived Diagnosis and Care Recommendations. View Abstract
Effect of Angiofibromas on Quality of Life and Access to Care in Tuberous Sclerosis Patients and Their Caregivers. View Abstract
Clinical Trial of the Protein Farnesylation Inhibitors Lonafarnib, Pravastatin, and Zoledronic Acid in Children With Hutchinson-Gilford Progeria Syndrome. View Abstract
A Widespread Pruritic Rash With Facial Swelling and Black Streaks. View Abstract
Gastrointestinal Infantile Hemangioma: Presentation and Management. View Abstract
Impact of Screening for Hepatic Hemangiomas in Patients with Multiple Cutaneous Infantile Hemangiomas. View Abstract
Distinct Cutaneous Manifestations and Cold-Induced Leukocyte Activation Associated With PLCG2 Mutations. View Abstract
Capillary-venous malformation in the upper limb. View Abstract
Diffuse capillary malformation in association with fetal pleural effusion: report of five patients. View Abstract
Rapidly involuting congenital hemangioma with fetal involution. View Abstract
Infantile and congenital hemangiomas. View Abstract
Frequency of ear symptoms and hearing loss in ichthyosis: a pilot survey study. View Abstract
Growth hormone replacement in patients with PHACE association and hypopituitarism. View Abstract
Pediatric melanoma, moles, and sun safety. View Abstract
Initial cutaneous manifestations of Hutchinson-Gilford progeria syndrome. View Abstract
Diffuse capillary malformation with overgrowth: a clinical subtype of vascular anomalies with hypertrophy. View Abstract
Capillary-venous malformation in the lower limb. View Abstract
Clinical trial of a farnesyltransferase inhibitor in children with Hutchinson-Gilford progeria syndrome. View Abstract
Picture of the month-quiz case. Infantile Fibrosarcoma. View Abstract
Kaposiform hemangioendothelioma: atypical features and risks of Kasabach-Merritt phenomenon in 107 referrals. View Abstract
Pathogenesis of infantile hemangiomas. View Abstract
Sweet syndrome in children. View Abstract
Severe atopic dermatitis and transient hypogammaglobulinemia in children. View Abstract
Management of capillary malformations. View Abstract
Vascular malformations. View Abstract
LUMBAR: association between cutaneous infantile hemangiomas of the lower body and regional congenital anomalies. View Abstract
Terminology used to describe vascular anomalies. View Abstract
A Chronic Rash with a "Wood Grain" Pattern on the Extremities View Abstract
Diffuse Capillary Malformation with Proportionate Overgrowth: Characterization of a Disorder Distinct from Defined Overgrowth Syndromes View Abstract
Glucose transporter-1 protein is immunohistochemically expressed in subglottic infantile haemangioma. View Abstract
What syndrome is this? Laryngo-onycho-cutaneous syndrome. View Abstract
Vascular Anomalies View Abstract
Gastrointestinal tract involvement in Langerhans cell histiocytosis: case report and literature review. View Abstract
Celiac disease presenting with chilblains in an adolescent girl. View Abstract
Hypopituitarism in PHACES Association. View Abstract
Congenital infantile fibrosarcoma: a masquerader of ulcerated hemangioma. View Abstract
Genuine diffuse phlebectasia of Bockenheimer: dissection of an eponym. View Abstract
Congenital Cutaneous Mastocytosis View Abstract
Pediatric Sweet Syndrome: A Case Series View Abstract
What syndrome is this? Sjögren-Larsson syndrome. View Abstract
D2-40 immunohistochemical analysis of pediatric vascular tumors reveals positivity in kaposiform hemangioendothelioma. View Abstract
Cutaneovisceral angiomatosis with thrombocytopenia. View Abstract
Kaposiform hemangioendothelioma without Kasabach-Merritt phenomenon. View Abstract
Characteristics of mycobacterial infection in patients with immunodeficiency and nuclear factor-kappaB essential modulator mutation, with or without ectodermal dysplasia. View Abstract
"But they told us she had a hemangioma...." View Abstract
Laryngo-onycho-cutaneous Syndrome in a Pakistani Female View Abstract
Accuracy in Terminology, Diagnosis and Management for Referrals to a Vascular Anomalies Center View Abstract
Congenital Infantile Fibrosarcoma Masquerading as an Ulcerated Hemangioma of Infancy View Abstract
PHACE Syndrome View Abstract
Cystic Fibrosis Presenting as a Diffuse Erythematous Scaly Eruption View Abstract
The Spectrum of Mycobacterial Infection in Patients with Immunodeficiency and NFkB Essential Modifier (NEMO) Mutation with or without Ectodermal Dysplasia View Abstract
Congenital Infantile Fibrosarcoma Masquerading as an Ulcerated Congenital Hemangioma View Abstract
Childhood bullous pemphigoid: a clinicopathologic study and review of the literature. View Abstract
Fibroblastic rheumatism: case report and review of the literature. View Abstract
Aggressive management of juvenile dermatomyositis results in improved outcome and decreased incidence of calcinosis. View Abstract
Perineal ulcerations as the presenting manifestation of hemangioma. View Abstract
Oral lesions View Abstract
Acral Papules, Polyarthritis and Induration of the Skin View Abstract
Progeria View Abstract
Cutaneous inoculation tuberculosis in a child. View Abstract
Familial Annular Erythema View Abstract
Cutaneous Tuberculosis in a Child View Abstract
Herpes Zoster Following Varicella Vaccination View Abstract
Herpes zoster after varicella immunization. View Abstract
Treatment of confluent and reticulated papillomatosis of Gougerot et Carteaud with minocycline View Abstract
Progressive Port-wine Stain in Phakomatosis Pigmentovascularis Type IIIa View Abstract
Perineal and lip ulcerations as the presenting manifestation of hemangioma of infancy. View Abstract
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