Alyaa Al-Ibraheemi, MD
Director of Surgical Pathology; Director of Patient Safety and Quality Assurance; Department of Pathology; Bone and Soft Tissue Pathology; Vascular Anomalies
Associate Professor of Pathology, Harvard Medical School
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Alyaa Al-Ibraheemi, MD
Director of Surgical Pathology; Director of Patient Safety and Quality Assurance; Department of Pathology; Bone and Soft Tissue Pathology; Vascular Anomalies
Associate Professor of Pathology, Harvard Medical School
Medical Services
Languages
Arabic
English
Education
Medical School
University of Baghdad, College of Medicine
2006
Baghdad
Iraq
Residency
University of Texas Medical School
2014
Houston
TX
Fellowship
Boston Children's Hospital
2015
Boston
MA
Fellowship
Mayo Clinic
2016
Rochester
MN
Certifications
American Board of Pathology (Anatomic Clinical Pathology)
American Board of Pathology (Pediatric)
Publications
Polyvinyl Alcohol Sponges Reduce Intraperitoneal Adhesions After Abdominal Surgery. View Abstract
Correction to: What is new in fibroblastic/myofibroblastic tumors in children. View Abstract
The Natural History of Congenital Hepatic Hemangiomas. View Abstract
Loss of H3K27me3 Is Not Specific to Malignant Triton Tumor: Immunohistochemical Analysis of 23 Cases of Embryonal Rhabdomyosarcoma. View Abstract
Pediatric-type Myoid Neoplasms of Somatic Soft Tissue: A Clinicopathological and Molecular Genetic Study of 78 Tumors, Highlighting Indolent Clinical Behavior and Frequent SRF Gene Rearrangements. View Abstract
Optimizing Ewing Sarcoma and Osteosarcoma Biopsy Acquisition: A Children's Oncology Group Bone Tumor Committee Consensus Statement. View Abstract
Advances in Pediatric Pathology: Bridging Innovation and Clinical Practice for Emerging Entities. View Abstract
Advances in vascular anomalies: refining classification in the molecular era. View Abstract
Pearls and Updates on Pediatric Tyrosine Kinase-Altered Tumors. View Abstract
What is new in fibroblastic/myofibroblastic tumors in children. View Abstract
Perivascular Epithelioid Cell-Family Tumors in Children, Adolescents, and Young Adults: Clinicopathologic Features in 70 Cases. View Abstract
Author Correction: Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. View Abstract
Early Graft Loss With Suspected Seventh-Day Syndrome Following Pediatric Liver Transplantation. View Abstract
ASPSCR1::TFE3 Drives Alveolar Soft Part Sarcoma by Inducing Targetable Transcriptional Programs. View Abstract
Molecular profiling of 888 pediatric tumors informs future precision trials and data-sharing initiatives in pediatric cancer. View Abstract
Ewing Sarcoma of the Female Genital Tract: Clinicopathologic Analysis of 21 Cases With an Emphasis on the Differential Diagnosis of Gynecologic Round Cell, Spindle, and Epithelioid Neoplasms. View Abstract
Immunohistochemical Expression of Lymphatic Endothelial Markers in Blue Rubber Bleb Nevus Syndrome. View Abstract
The Pathologic Diagnosis of Pediatric Soft Tissue Tumors in the Era of Molecular Medicine: The Sarcoma Pediatric Pathology Research Interest Group Perspective. View Abstract
Papillary Hemangioma Harbors Somatic GNA11 and GNAQ Mutations. View Abstract
ALK-Rearranged Epithelioid Mesenchymal Neoplasm: Expanding the Spectrum of Tyrosine Kinase-Altered Mesenchymal Tumors. View Abstract
CTNNB1 and APC Mutations in Sinonasal Myxoma : Expanding the Spectrum of Tumors Driven By WNT/ß-catenin Pathway. View Abstract
Lipoblastoma Arising in the Head and Neck: A Clinicopathologic Analysis of 20 Cases. View Abstract
Primary Adrenal Epithelioid Angiosarcoma: A Case Report. View Abstract
FGFR1 gene fusions in a subset of pediatric mesenchymal tumors: Expanding the genetic spectrum of tumors sharing histologic overlap with infantile fibrosarcoma and "NTRK-rearranged" spindle cell neoplasms. View Abstract
Spectrum of Liver Pathology in Dyskeratosis Congenita. View Abstract
Pathogenic variants in PIK3CA are associated with clinical phenotypes of kaposiform lymphangiomatosis, generalized lymphatic anomaly, and central conducting lymphatic anomaly. View Abstract
Genomic analysis reveals germline and somatic PDGFRB variants with clinical implications in familial infantile myofibromatosis. View Abstract
Genomic Patterns of Malignant Peripheral Nerve Sheath Tumor (MPNST) Evolution Correlate with Clinical Outcome and Are Detectable in Cell-Free DNA. View Abstract
Expanding the Spectrum of Perioral Myogenic Tumors in Pediatric Patients: An SRF::NCOA2 Fused Perivascular Tumor of the Philtrum. View Abstract
Rare FGFR Oncogenic Alterations in Sequenced Pediatric Solid and Brain Tumors Suggest FGFR Is a Relevant Molecular Target in Childhood Cancer. View Abstract
Primary Clear Cell Sarcoma of Bone: Clinicopathologic Study of a Rare Presentation. View Abstract
Addressing the diagnostic and therapeutic dilemmas of ovarian immature teratoma: Report from a clinicopathologic consensus conference. View Abstract
Molecular profiling identifies targeted therapy opportunities in pediatric solid cancer. View Abstract
Histologic characterization of paediatric mesenchymal neoplasms treated with kinase-targeted therapy. View Abstract
Kaposiform Lymphangiomatosis: Pathologic Aspects in 43 Patients. View Abstract
Cellular variant of kaposiform lymphangiomatosis: a report of three cases, expanding the morphologic and molecular genetic spectrum of this rare entity. View Abstract
Application of the Milan System for Reporting Salivary Gland Cytopathology in pediatric patients: An international, multi-institutional study. View Abstract
ALK rearrangements in infantile fibrosarcoma-like spindle cell tumours of soft tissue and kidney. View Abstract
Mesenchymal neoplasms with NTRK and other kinase gene alterations. View Abstract
Bockenheimer disease is associated with a TEK variant. View Abstract
Intracranial venous malformation masquerading as a meningioma in PI3KCA-related overgrowth spectrum disorder. View Abstract
Molecular Characterization of Inflammatory Tumors Facilitates Initiation of Effective Therapy. View Abstract
Verrucous Venous Malformation-Subcutaneous Variant. View Abstract
Liver Pathology, Including MOC31 Immunohistochemistry, in Congenital Tufting Enteropathy. View Abstract
Assessment of BCOR Internal Tandem Duplications in Pediatric Cancers by Targeted RNA Sequencing. View Abstract
Cytomorphologic Spectrum of SMARCB1-Deficient Soft Tissue Neoplasms. View Abstract
Undifferentiated Embryonal Sarcoma of the Liver With Rhabdoid Morphology Mimicking Carcinoma: Expanding the Morphologic Spectrum or a Distinct Variant? View Abstract
Novel BRAF gene fusions and activating point mutations in spindle cell sarcomas with histologic overlap with infantile fibrosarcoma. View Abstract
Vascular Anomalies of the Head and Neck: A Pediatric Overview. View Abstract
Novel variants in the stem cell niche factor WNT2B define the disease phenotype as a congenital enteropathy with ocular dysgenesis. View Abstract
Newcomers in Vascular Anomalies. View Abstract
Plexiform Myofibroblastoma: Clinicopathologic Analysis of 36 Cases of a Distinctive Benign Tumor of Soft Tissue Affecting Mainly Children and Young Adults. View Abstract
Lipoblastoma phenotype contains a somatic PIK3CA mutation. View Abstract
Arteriovenous malformation phenotype resembling congenital hemangioma contains KRAS mutations. View Abstract
Calcifying synovial sarcoma of the tongue with SS18 rearrangement: a rare variant in a rare location. View Abstract
Making the most of small samples: Optimization of tissue allocation of pediatric solid tumors for clinical and research use. View Abstract
Congenital Disseminated Pyogenic Granuloma: Characterization of an Aggressive Multisystemic Disorder. View Abstract
Recurrent RET gene fusions in paediatric spindle mesenchymal neoplasms. View Abstract
Genomics of MPNST (GeM) Consortium: Rationale and Study Design for Multi-Omic Characterization of NF1-Associated and Sporadic MPNSTs. View Abstract
Arteriovenous Malformation MAP2K1 Mutation Causes Local Cartilage Overgrowth by a Cell-Non Autonomous Mechanism. View Abstract
Genomic and Immunologic Characterization of INI1-Deficient Pediatric Cancers. View Abstract
Surgical Management of Fibroadipose Vascular Anomaly of the Lower Extremities. View Abstract
Recurrent and novel USP6 fusions in cranial fasciitis identified by targeted RNA sequencing. View Abstract
Clinical characterization and long-term outcomes in pediatric epithelioid hemangioendothelioma. View Abstract
Arteriovenous malformation associated with a HRAS mutation. View Abstract
Atypical lipomatous tumour/well-differentiated liposarcoma and de-differentiated liposarcoma in patients aged = 40 years: a study of 116 patients. View Abstract
A Distinctive Genomic and Immunohistochemical Profile for NOTCH3 and PDGFRB in Myofibroma With Diagnostic and Therapeutic Implications. View Abstract
Intramuscular fast-flow vascular anomaly contains somatic MAP2K1 and KRAS mutations. View Abstract
Fibroadipose Vascular Anomaly in the Upper Extremity: A Distinct Entity With Characteristic Clinical, Radiological, and Histopathological Findings. View Abstract
Imaging findings in epithelioid hemangioendothelioma. View Abstract
Expanding the Spectrum of Pediatric NTRK-rearranged Mesenchymal Tumors. View Abstract
Adipocytic tumors in Children: A contemporary review. View Abstract
A somatic activating NRAS variant associated with kaposiform lymphangiomatosis. View Abstract
Desmoplastic Small Round Cell Tumors With Atypical Presentations: A Report of 34 Cases. View Abstract
Aberrant receptor tyrosine kinase signaling in lipofibromatosis: a clinicopathological and molecular genetic study of 20 cases. View Abstract
Malignant Tenosynovial Giant Cell Tumor: The True "Synovial Sarcoma?" A Clinicopathologic, Immunohistochemical, and Molecular Cytogenetic Study of 10 Cases, Supporting Origin from Synoviocytes. View Abstract
Characterization of long-term outcomes for pediatric patients with epithelioid hemangioma. View Abstract
Superficial Solitary Fibrous Tumor: A Series of 26 Cases. View Abstract
Metastatic rhabdomyosarcoma mimicking autoimmune pancreatitis diagnosed by EUS-guided fine-needle biopsy. View Abstract
Giant Cell Tumor of Bone in Patients 55 Years and Older: A Study of 34 Patients. View Abstract
PTEN hamartoma of the soft tissue: the initial manifestation of an underlying PTEN hamartoma tumor syndrome in a 4-year-old female. View Abstract
Pediatric Non-vestibular Schwannoma. View Abstract
Sonographic Pulmonary Abnormalities in Fetuses With Hypoplastic Left Heart Syndrome and Intact Atrial Septum Undergoing Attempted Atrial Septostomy In Utero. View Abstract
Autoamputation of the Appendix Presenting as a Calcified Abdominal Mass Following Necrotizing Enterocolitis. View Abstract
Fibrous hamartoma of infancy: a clinicopathologic study of 145 cases, including 2 with sarcomatous features. View Abstract
Histologic Spectrum of Giant Cell Tumor (GCT) of Bone in Patients 18 Years of Age and Below: A Study of 63 Patients. View Abstract
Plasmodium Falciparum Recurrence Two Years after Exposure in Endemic Country: A Case Report. View Abstract
Voluntary Second Opinions in Pediatric Bone and Soft Tissue Pathology: A Retrospective Review of 1601 Cases From a Single Mesenchymal Tumor Consultation Service. View Abstract
PPP6R3-USP6 amplification: Novel oncogenic mechanism in malignant nodular fasciitis. View Abstract
Comparison of Controlled Attenuation Parameter and Liver Biopsy to Assess Hepatic Steatosis in Pediatric Patients. View Abstract
Autoamputation of the appendix presenting as a calcified abdominal mass following necrotizing enterocolitis. View Abstract
Selected Diagnostically Challenging Pediatric Soft Tissue Tumors. View Abstract
TP53 overexpression is an independent adverse prognostic factor in de novo myelodysplastic syndromes with fibrosis. View Abstract
Comparison between 1-needle technique versus 2-needle technique for bone marrow aspiration and biopsy procedures. View Abstract
Phenotypic evolution in a case of peripheral T-cell lymphoma suggests the presence of tumor heterogeneity. View Abstract
BizarreParosteal Osteochondromatous Proliferation (Nora's lesion) with translocation t(1;17)(q32;q21): a case report and role of cytogenetic studies on diagnosis. View Abstract
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