Patel Paras, Amar Jaspreet, Poletto Erica
Final Pr. ID: Poster #: EDU-070
Marrow signal changes in the pediatric population are often complex and can appear nonspecific to the inexperienced radiologist. Normal physiological marrow changes from birth to adulthood play a confounding role. A good understanding for diffuse marrow replacing processes that demonstrate T1 hypointense signal on MRI is crucial for the radiologist to correctly identify pathology, provide early and pathology-specific treatment, and ultimately play a profound role in patient care. The purpose of this educational exhibit is to review the various pathological etiologies of diffuse T1 hypointense marrow signal changes in the pediatric patient, including sickle cell anemia, gaucher’s disease, leukemia, diffuse marrow metastasis, osteomyelitis, thalassemia, juvenile inflammatory arthritis, and bone marrow edema syndromes. Additionally, potential pitfalls will be discussed including red marrow hyperplasia, treatment related changes, immobilization/stress reaction, and normal residual red marrow. Case examples will be provided along with pearls that will aid the radiologist in narrowing their differential diagnosis when faced with specific clinical scenarios. Read More
Authors: Patel Paras , Amar Jaspreet , Poletto Erica
Keywords: Bone, Marrow, Pathological
Pace Erika, Clarke Enrico, Mandeville Henry, De Souza Nandita
Final Pr. ID: Paper #: 149
To measure and compare early (within 3 months) and late (beyond 3 months) changes in ADC of the clival marrow post-photon and proton therapy. Read More
Authors: Pace Erika , Clarke Enrico , Mandeville Henry , De Souza Nandita
Keywords: bone marrow, radiotherapy, proton beam therapy
Pace Erika, Vaidya Sucheta, De Souza Nandita
Final Pr. ID: Paper #: 150
To measure early (within 3 months) and late (beyond 3 months) changes in ADC of the lumbosacral vertebral marrow following chemotherapy in children with abdomino-pelvic neoplasms and interpret them in the context of ADC measurement reproducibility. Read More
Authors: Pace Erika , Vaidya Sucheta , De Souza Nandita
Keywords: bone marrow, chemotherapy, abdomino-pelvic neoplasm
Miller Stephen, Scrugham Jeffrey, Pivnick Eniko
Final Pr. ID: Poster #: CR-080
Congenital generalized lipodystrophy, also known as Berardinelli-Seip syndrome, is a rare autosomal recessive disorder associated with osteosclerosis and cystic intramedullary bone lesions. However, the transition from generalized osteosclerosis in the young patient to the development of cystic intramedullary bone lesions in areas converting from red to yellow marrow in the growing child has not been previously described. We present a young man with congenital generalized lipodystrophy, followed in our clinic from age 5 years through age 14 years, and document the development over time of dramatic cystic lesions within previously sclerotic long bones. The location of these intramedullary bone cysts appears to mirror the transition of red (hematopoietic) to yellow (fatty) marrow in the maturing child. Recognition of this pattern may affect recommended physical activity and subsequent orthopedic management. Read More
Authors: Miller Stephen , Scrugham Jeffrey , Pivnick Eniko
Keywords: lipodystrophy, bone cyst, marrow
Alis Jonathan, Levin Terry, Kurian Jessica, Mahadeo Kris, Taragin Benjamin
Final Pr. ID: Poster #: EDU-092
Sickle Cell Disease (SCD) affects approximately 100,000 individuals in the US. Despite medical advances, morbidity is high and their lifespan remains shortened. Hematopoietic stem cell transplantation (HSCT) is the only curative treatment to date and as outcomes improve its use has increased. Complications of HSCT are frequent and some literature suggests there is a higher incidence in the SCD population. In addition, preexisting vasculopathy in this population may contribute to an increased incidence of post-transplant CNS toxicity. We present the imaging findings of HCST complications in children with SCD. Read More
Authors: Alis Jonathan , Levin Terry , Kurian Jessica , Mahadeo Kris , Taragin Benjamin
Keywords: Graft versus host disease, bone marrow transplant, HSCT
Degnan Andrew, Serai Suraj, Ho-fung Victor, Barrera Christian, Wang Dah-jyuu, Ahrens-nicklas Rebecca, Ficicioglu Can
Final Pr. ID: Poster #: EDU-057
Gaucher disease is an inherited metabolic disorder due deficiency of the lysosomal enzyme β-glucocerebrosidase that results in the accumulation of abnormal macrophages (“Gaucher cells”) within multiple organs, most conspicuously affecting the liver, spleen and bone marrow. As the diagnosis is increasingly made during childhood and young adulthood, pediatric radiologists should be familiar with imaging features of Gaucher disease and its complications.
Visceromegaly consisting of hepatosplenomegaly is a hallmark of Gaucher disease and uniformly present in cohorts of pediatric patients. In addition, bone marrow involvement with ‘Erlenmeyer flasks’ have been long recognized as part of this disease, although the classic radiographic finding is not present until adulthood. Marrow involvement confers significant morbidity for these patients with pain, bone infarcts and pathologic fracture.
Traditionally, imaging of disease severity has been based on hepatic and splenic visceral organ enlargement and/or qualitative assessment of bone marrow involvement. However, advances in the understanding of Gaucher disease and observations of elevated ferritin levels and increased risk of hepatic fibrosis emphasize the importance of more comprehensive assessment of liver involvement beyond simple enlargement. Moreover, quantitative MRI assessment of bone fat-fractions also may have a role in assessing marrow involvement. These methods of disease assessment are important in addressing management decisions regarding enzyme replacement and substrate reduction therapy.
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Authors: Degnan Andrew , Serai Suraj , Ho-fung Victor , Barrera Christian , Wang Dah-jyuu , Ahrens-nicklas Rebecca , Ficicioglu Can
Keywords: Gaucher disease, bone marrow, hepatic involvement
Medina Perez Mariangeles, Gupta Saurabh, Salastekar Ninad, Badar Zain, Majmudar Anand
Final Pr. ID: Poster #: EDU-059
Bone marrow is composed of fat and cellular elements supported by the trabecular bone. Pathological lesions of the bone marrow usually replace its normal constituent to a variable degree. Differentiation among traumatic, neoplastic, and inflammatory processes of the bone marrow is often not possible with MRI, which commonly requires the patient to undergo additional invasive diagnostic procedures to obtain an accurate diagnosis.
In-phase and opposed-phase imaging has been used extensively in imaging of the liver and adrenal glands. However, recently it has been introduced into the evaluation of the bone marrow. The technique takes advantage of different excitation frequencies of water and fat protons due to differences in their molecular environments. The main concept is that the presence of normal bone marrow would result in suppression of signal intensity on the opposed-phase images. In the presence of infiltration lesions of the bone marrow, normal fat-containing marrow will be replaced with neoplastic cells and result in lack of suppression on the opposed-phase images.
The main teaching purpose of this exhibit will be to demonstrate, by a pictorial case-based review, the appearance of multiple cases of biopsy-proven infiltrating lesions of the bone marrow, and emphasize how they can be differentiated from other traumatic or inflammatory processes.
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Authors: Medina Perez Mariangeles , Gupta Saurabh , Salastekar Ninad , Badar Zain , Majmudar Anand
Keywords: In-phase, opposed-phase, marrow
Raissaki Maria, Demetriou Stelios, Skiadas Christos, Spanakis Kostas, Stratigaki Maria, Katzilakis Nikos, Stiakaki Eftichia, Karantanas Apostolos
Final Pr. ID: Poster #: EDU-012
There are various conditions or diseases that may cause multiple bone marrow lesions in children or adolescents. Radiographically, lytic lesions may become apparent after loss of >50% of bone mineral content. Scintigraphy requires osteoblastic activity and is not specific. MRI has been increasingly employed for the investigation of diseases that involve the skeleton and for further delineation of radiographic findings in symptomatic children.
Purpose: To describe the MRI findings of entities resulting in multiple bone marrow lesions in children and provide a wide differential diagnosis.
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Authors: Raissaki Maria , Demetriou Stelios , Skiadas Christos , Spanakis Kostas , Stratigaki Maria , Katzilakis Nikos , Stiakaki Eftichia , Karantanas Apostolos
Keywords: bone marrow, polyostotic, multifocal bone lesions, mri
Final Pr. ID: Poster #: EDU-035
The purpose of this educational exhibit is to describe the most common pediatric bone marrow patterns, including normal variants and common pathology. Read More
Authors: Kelleher Michael
Keywords: MR, Bone marrow
Samet Jonathan, Schafernak Kristian, Arva Nicoleta, Deng Jie
Final Pr. ID: Poster #: SCI-049
MRI interpretation of pediatric bone marrow is a challenging task due to the highly variable appearance. The bone marrow composition, especially the cellularity, changes with age, benign and malignant hematologic conditions, medications, among other etiologies. Detection of a marrow replacement process on MRI can be missed even by experienced radiologists. Normal hematopoietic bone marrow from birth to 9 years ranges from 20-40% fat (inversely related to cellularity). In malignant marrow replacement processes such as leukemia, bone marrow is highly cellular and fat percentage is low. Currently, no technique is routinely used in clinical practice to quantify bone marrow fat percentage on MRI. Read More
Authors: Samet Jonathan , Schafernak Kristian , Arva Nicoleta , Deng Jie
Keywords: Bone Marrow, Fat fraction, leukemia
Final Pr. ID: Paper #: 151
To establish the reproducibility of the apparent diffusion coefficient (ADC) measurement in the bone marrow of the clivus and lumbosacral spine. Read More
Authors: Pace Erika , De Souza Nandita
Keywords: bone marrow, reproducibility, apparent diffusion coefficient