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A rare case of FH-deficient renal cell carcinoma with signet ring cells features.
Diagn Pathol
December 2024
Shenzhen Hospital, National Cancer Center, National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Fumarate hydratase-deficient renal cell carcinoma (FH-deficient RCC) is a clinically aggressive tumor with high rates of progression and mortality. A wide range of morphological variations has been observed in FH-deficient RCC, initially described as type 2 papillary RCC or unclassified RCC. Here, we report a case of FH-deficient RCC with rare signet ring cells features.
View Article and Find Full Text PDFMulti-segmental zosteriform leiomyoma cutis: a rare cutaneous neoplasm.
BMJ Case Rep
November 2024
Dermatology, Dr D Y Patil Vidyapeeth (Deemed to be University), Pune, Maharashtra, India.
Single-Port Versus Reduced-Port (1 + 1) Robotic Myomectomy and Hysterectomy.
J Clin Med
October 2024
Department of Obstetrics & Gynecology, College of Medicine, The Catholic University of Korea, 222 Banpo-daero, Seocho-gu, Seoul 06591, Republic of Korea.
Article Synopsis
- The study compared reduced-port (RP) robotic surgery to single-port (SP) robotic surgery by analyzing outcomes from 184 patients who underwent either myomectomy or hysterectomy.
- Results showed that RP robotic surgery was effective, with more leiomyomas removed in the RP robotic myomectomy (RP-RM) group compared to the SP-RM group.
- Overall, RP robotic surgery was found to be a feasible alternative to SP surgery, with shorter operating times for RP robotic hysterectomy (RP-RH) compared to SP robotic hysterectomy (SP-RH).
Rapid identification of primary atopic disorders (PAD) by a clinical landmark-guided, upfront use of genomic sequencing.
Allergol Select
October 2024
Center for Child and Adolescent Health, Helios Hospital Krefeld, Academic Hospital of RWTH Aachen, Krefeld.
Article Synopsis
- Primary atopic disorders (PAD) are rare genetic conditions caused by specific gene variants that affect skin and immune function, making diagnosis challenging among common allergic disease cases.
- Identifying PAD requires recognizing clinical red flags like family history and unusual infections, as conventional lab tests are inadequate for definitive diagnosis.
- Whole-genome sequencing (WGS) enhances diagnostic efficiency and accuracy, but requires careful interpretation and collaboration among specialists to effectively manage PAD cases.
Genetic Predisposition for Gynecologic Cancers.
Clin Obstet Gynecol
December 2024
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Comprehensive Cancer Center, University of Virginia Health, Charlottesville, Virginia.
Article Synopsis
- Hereditary cancer syndromes account for up to 10% of all cancers and are often detected after a cancer diagnosis, indicating a need for earlier testing.
- Primary care providers, especially obstetrician-gynecologists, can play a crucial role in assessing hereditary cancer risks through family history and genetic testing.
- Identifying hereditary cancer genes can lead to proactive prevention strategies, including better screenings and personalized care plans, particularly for common gynecologic hereditary cancer syndromes.
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