Results 51 to 60 of about 8,625,025 (271)

Reviving the Rarity of Cecal Lymphangioma: A Case Report

Cureus
The present case report describes the incidental discovery of cecal lymphangioma, a rare benign neoplasm originating from malformations of lymphatic vessels. Lymphangiomas are uncommon in the gastrointestinal tract, and their presence in the colon is particularly unusual.
Eppley, David A, Rana, Zaid
openaire   +2 more sources

Ovarian Sex Cord Stromal Tumors in Children and Adolescents—The European Standard Clinical Practice Recommendations

Pediatric Blood &Cancer, EarlyView.
ABSTRACT As part of the European Cooperative Study Group for Paediatric Rare Tumours initiative, we developed standard clinical practice guidelines for ovarian sex cord stromal tumors, based on comprehensive national and international cohort analyses, literature review, and a final expert consensus conference.
Dominik T. Schneider, Kris‐Ann Schultz, Nora Schnitzler, Michael Abele, Tal Ben‐Ami, Ewa Bien, Gianni Bisogno, Ines B. Brecht, Maja Cesen, Andrea Ferrari, Michaela Kuhlen, Malgorzata A. Krawczyk, Ricardo Lopez‐Almaraz, Yves Reguerre, Calogero Virgone, Daniel Orbach   +15 more
wiley   +1 more source

Lipoma; a rarity in the oral cavity: a case report

Journal of Oral Medicine, Oral Surgery, Oral Pathology and Oral Radiology, 2016
Lipomas are rare, benign tumours of mesenchymal origin, representing 1–5% of all benign oral tumors. Clinically, intraoral lipomas present as slow growing, soft, asymptomatic mass. Histopathologically, they are composed predominantly of mature adipocytes admixed with collagenous tissue and may be surrounded by a thin fibrous capsule.
Ankit Srivastava, K.R. Vijayalakshmi, Mubeen Khan   +2 more
openaire   +1 more source

Rarity among the rare-large and invasive thymoma, a case report and review [PDF]

Journal of Community Hospital Internal Medicine Perspectives, 2020
Thymomas are rare tumors of the thymic epithelium with an incidence of 1.5 cases in a million, with a wide spectrum of morphological, pathologic characteristics, and clinical presentations. Despite its benign histological appearance, it can invade nearby structures or metastasize hence clinicians need to have a high index of suspicion for early ...
Khadija Tayabali, Hussein Pothiwalla, Jason Thole, Binh Nguyen   +3 more
openaire   +3 more sources

Central Nervous System Tumors Among Infants in Canada: A Report From CYP‐C

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Central nervous system (CNS) tumors in infants are rare, pose unique clinical challenges, and lack large‐scale evidence‐based data to guide management. This study seeks to describe CNS tumors in Canadian infants and to compare their outcomes with those of older children.
Samuel Sassine, Hallie Coltin, Sylvia Cheng, Lucie Lafay‐Cousin, Vanan Issai Magimairajan, Craig Erker, Stéphanie Vairy, Lynette Bowes, Adam Fleming, Donna Johnston, Sarah McKillop, Roona Sinha, Julie Bennett, Christina Coleman, Laura Wheaton, Shayna Zelcer, Samuele Renzi, Thai Hoa Tran   +17 more
wiley   +1 more source

Impact of Radiation Therapy on Physical and Psychosocial Health of Adolescents and Young Adults: A Joint Report From the Children's Oncology Group AYA and Radiation Oncology Committees

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Rates of cancer among adolescents and young adults (AYA), age 15–39 years, are increasing. Consequently, radiation oncologists are treating more AYAs who have diagnoses spanning both pediatric and adult practices. Compared to pediatric and older adult patients, AYAs face a unique set of challenges.
Hesham Elhalawani, Rachel K. Peterson, Avani D. Rao, Laurie J. McKenzie, Ahmed Magdy Elmotayam, Leslie Chang, Michael Roth, Susan L. McGovern   +7 more
wiley   +1 more source

Double trouble – A twin rarity in the same patient

Kerala Journal of Ophthalmology
Detecting a rare finding is always a source of excitement in a clinician’s practice. This in turn leads to unearthing and learning more about the disease detected.
Allen Mathew
doaj   +1 more source

Unfolding the rarity of SMARCA4 deficient uterine sarcoma (SDUS): A case report

Gynecologic Oncology Reports, 2021
SMARCA4 deficient uterine sarcoma (SDUS) is a relatively new entity added to the family of uterine sarcoma characterised by SMARCA4/BRG1 deficiency.A 62 years old lady presented with abdominal pain and vaginal discharge. On evaluation, found to have a pelvic mass with lymph nodal involvement.
Annie Kanchan Baa, Sameer Rastogi, Sarthak Tripathy, Shamim Ahmed Shamim, Santosh Menon   +4 more
openaire   +3 more sources

Retrospective Analysis of Donor Lymphocyte Infusions in Pediatric Patients With Mixed Chimerism After Hematopoietic Stem Cell Transplantation

Pediatric Blood &Cancer, EarlyView.
ABSTRACT Background Allogeneic hematopoietic stem cell transplantation (alloHSCT) is an essential therapy for several malignant and nonmalignant diseases, but relapse and graft loss remain the principal threats to its success. Routine monitoring of chimerism and minimal residual disease (MRD) enables early detection of imminent recurrence and guides ...
Carmen Junk, Sebastian Michaelis, Michaela Döring, Thomas Eichholz, Ursula Holzer, Martin Ebinger, Tim Flaadt, Rupert Handgretinger, Peter Lang, Jan Frederic Weller, Markus Mezger   +10 more
wiley   +1 more source

Non-Hodgkin′s lymphoma "masquerading" as Pott′s disease in a 13-year old boy

Indian Journal of Medical and Paediatric Oncology, 2011
Lymphomas are malignant neoplasms of the lymphoid lineage. They are broadly classified as either Hodgkin disease or as non-Hodgkin lymphoma (NHL). Burkitt′s lymphoma, a variety of NHL, is significantly most common in sub-Saharan Africa, where it accounts
Olasunkanmi Abdulrasheed Adegboye
doaj   +1 more source