Cargando…

Prepubertal Idiopathic Unilateral Gynecomastia: Case Report and Literature Review

INTRODUCTION: Gynecomastia is a benign proliferation of the glandular tissue of the breast in males. Depending on the age, it can be considered a physiological condition. Prepubertal unilateral gynecomastia is a rare phenomenon. There are only a few case reports described through the last few years....

Descripción completa

Detalles Bibliográficos
Autores principales:	Herbert, Saskia-Laureen, Ergezinger, Katrin, Sauer, Stephanie, Kurz, Florian, Schlaiß, Tanja, Wöckel, Achim, Albert, Ute-Susann
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	S. Karger AG 2022
Materias:	Novel Insights from Clinical Practice
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9801404/ https://www.ncbi.nlm.nih.gov/pubmed/36590144 http://dx.doi.org/10.1159/000525096

Ejemplares similares

Severe Brain Damage in a Moderate Preterm Infant as Complication of Post-COVID-19 Response during Pregnancy
por: Engert, Viktoria, et al.
Publicado: (2021)

Idiopathic prepubertal unilateral gynecomastia: Case report and literature review
por: Wang, Chenyu, et al.
Publicado: (2019)

Prepubertal unilateral gynecomastia in the absence of endocrine abnormalities
por: Kang, Min, et al.
Publicado: (2014)

Clinical and surgical management of unilateral prepubertal gynecomastia
por: Ferraro, Giuseppe Andrea, et al.
Publicado: (2014)

Prepubertal Unilateral Gynecomastia: Report of 2 Cases
por: Demirbilek, Hüseyin, et al.
Publicado: (2014)

Prepubertal unilateral gynecomastia: a report of two cases
por: Hoevenaren, Inge A., et al.
Publicado: (2010)

A New, Atypical Case of Cobalamin F Disorder Diagnosed by Whole Exome Sequencing
por: Constantinou, Panayiotis, et al.
Publicado: (2016)

Coexistence of Mosaic Uniparental Isodisomy and a KCNJ11 Mutation Presenting as Diffuse Congenital Hyperinsulinism and Hemihypertrophy
por: Kocaay, Pınar, et al.
Publicado: (2016)

Erroneously High Lactate: A Guide to Diagnosing Ethylene Glycol Poisoning
por: Kamboj, Mayanka, et al.
Publicado: (2019)

Primary Pulmonary MALT Lymphoma: A Case Report and Literature Review
por: Couto, Carlos, et al.
Publicado: (2019)

Migration of an Ingested Fish Bone to the Submandibular Gland: A Case Report and Literature Review
por: Ma, Jinhua, et al.
Publicado: (2019)

Rapid Progression of Tracheoesophageal Fistula Caused by Immunotherapy Administered after Tracheal Stent Placement
por: Mizuguchi, Shinjiro, et al.
Publicado: (2019)

Asymptomatic Dialysate Turbidity and Repeated Intraductal Clots in a Peritoneal Dialysis Patient
por: Xu, Tian, et al.
Publicado: (2019)

An Unusual Tooth Shedding with Internal Resorption: A Case Report
por: Ngoc, Vo Truong Nhu, et al.
Publicado: (2019)

Nasal Cavity Paraganglioma: Literature Review and Discussion of a Rare Case
por: de Almeida Vital, Juliana Maria, et al.
Publicado: (2017)

Rapid Regression of Obstructive Cardiac Rhabdomyoma in a Preterm Neonate after Sirolimus Therapy
por: Lee, Seung Jae, et al.
Publicado: (2017)

Repigmentation of White Forelock in a Familial Case of Piebaldism Reported via Teledermatology in the COVID-19 Era
por: Gaudiello, Francesca, et al.
Publicado: (2021)

Telogen Effluvium after SARS-CoV-2 Infection: A Series of Cases and Possible Pathogenetic Mechanisms
por: Rossi, Alfredo, et al.
Publicado: (2021)

Potential Role of the Galectin-9/TIM-3 Axis in the Disparate Progression of SARS-CoV-2 in a Married Couple: A Case Report
por: Martín-Quirós, Alejandro, et al.
Publicado: (2021)

Persistent Hypoglycemia with Polycystic Kidneys: A Rare Combination − A Case Report
por: Prasher, Priya, et al.
Publicado: (2020)

Intraductal Carcinoma of the Parotid Gland Presenting as Parapharyngeal Mass
por: Oki, Yamato, et al.
Publicado: (2020)

Infantile Pyknocytosis: End-Tidal CO, %Micro-R Measurements, Next-Generation Sequencing, and Transfusion Avoidance with Darbepoetin
por: Bahr, Timothy M., et al.
Publicado: (2020)

Vaccine Toes Are the New COVID Toes
por: Hodge, Bonnie, et al.
Publicado: (2022)

Primary Mediastinal Large B-Cell Lymphoma Achieved by Non-Cautery Assisted Transbronchial Mediastinal Cryobiopsy
por: Zhang, Jing, et al.
Publicado: (2022)

Exome Sequencing Identifies a Novel SIN3A Variant in a Patient with Witteveen-Kolk Syndrome
por: Penon-Portmann, Monica, et al.
Publicado: (2022)

A Case Report on Cannabinoid Hyperemesis Syndrome in Palliative Care: How Good Intentions Can Go Wrong
por: Senderovich, Helen, et al.
Publicado: (2022)

Treatment of Fingernail Onychomycosis with Efinaconazole 10% Solution in a Patient with Scleroderma: A Case Report
por: Miller, Rhiannon C., et al.
Publicado: (2022)

Ocular Manifestations of Hurler-Scheie Syndrome: Recurrence of Host Disease in the Corneal Transplant
por: Kölkedi, Zsófia, et al.
Publicado: (2023)

Basal Cell Adenocarcinoma Arising from the Parotid Gland
por: Vitorino, Marina, et al.
Publicado: (2022)

SARS-CoV-2 Infection of Young Infants during the Omicron Wave: A Case Series
por: Sehr Ansari, Najmus, et al.
Publicado: (2023)

Alopecia Areata after COVID-19 Vaccines
por: Genco, Lucia, et al.
Publicado: (2023)

Interstitial Pulmonary Fibrosis and Extensive Dendriform Ossification with Persistent Viral Load: A Rare Presentation of Post-COVID-19 Condition in Need of Lung Transplantation
por: Haslbauer, Jasmin Dionne, et al.
Publicado: (2023)

Fibular Agenesis and Ball-Like Toes Mimicking Preaxial Polydactyly: Prenatal Presentation of Du Pan Syndrome
por: Turgut, G. Tutku, et al.
Publicado: (2023)

Severe Emphysema Treated with Bilateral Lung Sealant: A Case Series with Long-Term Follow-Up
por: Lindnér, Cecilia, et al.
Publicado: (2023)

Endoscopic Third Ventriculostomy with Choroid Plexus Cauterization in Infantile Hydrocephalus: An Experience from Mali
por: Diallo, Oumar, et al.
Publicado: (2023)

Review of Pediatric Extraosseous Chordomas with a Unique, Illustrative Case
por: Lee, Benjamin J., et al.
Publicado: (2023)

Primary Effusion Lymphoma in an HIV-Negative Patient with Chronic Myeloid Leukemia Treated with Dasatinib
por: SahBandar, Ivo N., et al.
Publicado: (2023)

Warfarin-Associated Fetal Subdural Hematoma Causing Severe Neurodevelopmental Delay: A Case Report
por: Safra, Ibrahim, et al.
Publicado: (2023)

Triosephosphate Isomerase Deficiency: E105D Mutation in Unrelated Patients and Review of the Literature
por: Selamioğlu, Arzu, et al.
Publicado: (2023)

Differential Diagnosis of Pulmonary Veno-Occlusive Disease and/or Pulmonary Capillary Hemangiomatosis after Identification of Two Novel EIF2AK4 Variants by Whole-Exome Sequencing
por: Park, Jong Eun, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_5n24e5n2ic67ucv49lnukn2mv2