Results 71 to 80 of about 6,776 (214)

Lipomatous retroperitoneal ganglioneuroma

Muller Journal of Medical Sciences and Research, 2015
Fatty replacement of non-lipomatous tumors is rare. We report a case of retroperitoneal ganglioneuroma, showing fatty replacement in a 17-year-old adolescent male. The patient presented with a left lumbar mass.
Rama Srivastava, Smriti Agnihotri, Nandyala Hari Sarma   +2 more
doaj   +1 more source

Atypical Neuroblastoma With Absent Urinary Catecholamine Excretion and 123ImIBG Avidity Are of Favorable Outcome: A Retrospective French Single‐Center Study

Pediatric Blood &Cancer, Volume 72, Issue 11, November 2025.
Abstract Background In neuroblastoma (NB), urinary catecholamine excretion and 123ImIBG avidity—depending on tumor enzymatic activity and norepinephrine transporter expression, respectively—are diagnostic standards. The prognostic impact of atypical NB, without urinary catecholamine excretion and/or 123ImIBG avidity, remains to be determined. We sought
Anna Borovkov, Juliette Assy, Isabelle Aerts, Franck Bourdeaut, Camille Cordero, Valérie Laurence, Amaury Leruste, Sarah Winter, Jean Michon, Daniel Orbach, Hélène Pacquement, Pascale Philippe‐Chomette, Gaelle Pierron, Julien Masliah‐Planchon, Sylvie Helfre, Isabelle Janoueix‐Lerosey, Anne‐Sophie Defachelles, Claudia Pasqualini, Nina Jehanno, Joanna Cyrta, Arnaud Gauthier, Véronique Mosseri, François Doz, Sabine Sarnacki, Liesbeth Cardoen, Hervé J. Brisse, Marie Luporsi, Gudrun Schleiermacher   +27 more
wiley   +1 more source

Phaeochromocytoma Associated to Von Recklinghausen Neurofibromatosis Type I: a Rare Clinical Case [PDF]

, 2011
Os feocromocitomas são neoplasias originárias das células cromafins da crista neural localizados, na sua grande maioria, na medula supra-renal, podendo também aparecer nos gânglios simpáticos (paragangliomas).
Jorge, V, Noronha, C, Pires da Silva, I, Riscado, M, Sousa, M   +4 more
core  

Mielolipoma adrenal gigante associado à deficiência da 21-hidroxilase: associação não usual simulando um carcinoma adrenocortical secretor de androgênios [PDF]

, 2010
The objective of this study was to describe a case of giant myelolipoma associated with undiagnosed congenital adrenal hyperplasia (CAH) due to 21-hydroxylase (21OH) deficiency.
CASTRO, Margaret de, ELIAS JUNIOR, Jorge, ELIAS, Paula C. Lamparelli, MERMEJO, Lívia Mara, MOREIRA, Ayrton Custódio, SAGGIORO, Fabiano Pinto, TUCCI JUNIOR, Silvio   +6 more
core   +2 more sources

Cystathionine as a Potential Urinary Marker for Diagnosing and Assessing Pretreatment Risk in Neuroblastoma

Cancer Science, Volume 116, Issue 11, Page 3102-3112, November 2025.
This study examined cystathionine as a new candidate marker for neuroblastoma and evaluated its utility as a biomarker for the diagnosis and pretreatment risk assessment of neuroblastoma through quantitative analyses of urine samples from control participants and patients with neuroblastoma.
Hizuru Amano, Yoshiharu Hayashi, Kazuharu Harada, Atsushi Narita, Shigehisa Fumino, Yuji Yamada, Shuhei Karakawa, Minoru Sakairi, Chiyoe Shirota, Takahisa Tainaka, Kazuki Yokota, Satoshi Makita, Daiki Kato, Hiroki Ishii, Kyoichi Deie, Makiko Mori, Yuichi Mitani, Yutaka Tomioka, Masataka Taguri, Katsuyoshi Koh, Tatsuro Tajiri, Motohiro Kato, Kimikazu Matsumoto, Yoshiyuki Takahashi, Tomoko Iehara, Akinari Hinoki, Hiroo Uchida   +26 more
wiley   +1 more source

Retroperitoneal ganglioneuroma

, 2009
Nöroblastom, ganglionöroblastom ve ganglionörom sempatik sinir sistemini oluşturan, değişik derecelerde olgunlaşmış, primordial nöral krest hücrelerinden köken alan heterojen bir grup tümördür. Abdominal distansiyon, sol üst kadran ağrısı ve daire şikayetleriyle başvuran 12 yaşındaki erkek hastaya yapılan tetkikler sonucu rastlantısal olarak primer ...
AKTOZ, Tevfik, KAPLAN, Mustafa, USTA, Ufuk, ATAKAN, İrfan Hüseyin, İNCİ, Osman   +4 more
openaire   +2 more sources

Paediatric parapharyngeal ganglioneuroma

BMJ Case Reports, 2018
A 17-year-old man initially presented to his primary care physician with throat pain for 1 week and was started on amoxicillin. After four additional days of ongoing pain and difficulty swallowing with decreased oral intake, he presented to the emergency department.
Jennifer Bach, Qazi Azher, Anas Salih
openaire   +3 more sources

Transoral excision of parapharyngeal ganglioneuroma

Journal of Pediatric Surgery Case Reports, 2020
Parapharyngeal space tumors are rare, where they represent only 0.5% of all head and neck tumors. This paper describes a rare case of a ganglioneuroma isolated in the paraphayngeal space.
Malak Almalki, Alanoud Hakami, Abdullah Arafat, Abdullah Albdah, Jaber Alshammri   +4 more
doaj   +1 more source

Deep Phenotyping of Pathology‐Confirmed Benign Lesions in PTEN Hamartoma Tumor Syndrome Patients

Clinical Genetics, Volume 108, Issue 4, Page 400-411, October 2025.
Gastrointestinal, skin, thyroid, and vascular lesions are frequently present in PTEN Hamartoma Tumor Syndrome patients with little to no difference between sexes or by index status. Early‐onset lipomas (< 20 years) may be useful for early recognition of patients, and uterine polyps should be considered for inclusion as a PHTS‐related lesion.
Ane J. Schei‐Andersen, Janneke H. M. Schuurs‐Hoeijmakers, Rachel van der Post, Arjen R. Mensenkamp, Jolanda Schieving, PTEN Study Group, Muriel A. Adank, Mirjam de Jong, Marjolijn C.J. Jongemans, Liselotte P. van Hest, Yvette van Ierland, Edward M. Leter, Maartje Nielsen, Janet R. Vos, Nicoline Hoogerbrugge   +14 more
wiley   +1 more source

Risk Assessment and Fertility Counseling for Hereditary Gynecological Cancer Syndromes

Cancer Medicine, Volume 14, Issue 17, September 2025.
ABSTRACT Objective To review the genetic basis, clinical characteristics, and management strategies of hereditary gynecologic cancers associated with hereditary cancer syndromes. Methods Literature on germline mutations, inheritance patterns, clinical manifestations, and fertility preservation strategies was reviewed.
Mei Zhao, Xiao‐ming Teng, Qiang Yan, Fan Hao   +3 more
wiley   +1 more source