keyword
https://read.qxmd.com/read/38552374/the-devastating-impact-of-unresectable-infectious-undifferentiated-pleomorphic-sarcoma-in-the-gluteal-region-a-case-report
#21
Rasoul Goli, Aysan Torabzadeh, Amireh Hassanpour, Alireza Jafarimaraghoush, Elaheh Manouchehri, Navid Faraji
INTRODUCTION AND IMPORTANCE: Undifferentiated pleomorphic sarcoma (UPS), previously known as malignant fibrous histiocytoma (MFH), is a highly aggressive soft tissue sarcoma characterized by its pleomorphic histology and lack of differentiation. CASE PRESENTATION: A 35-year-old man visited our oncology department with a complaint of a growing mass in his left buttock area. The mass had been increasing in size for the past six months, affected by local and systemic infection...
March 27, 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38550405/ovarian-cystic-lymphangioma
#22
Akanksha Sharma, Shivanjali Raghuvanshi, Manish Kumar, Nisha Singh, Nancy Gupta, Arina Alam, Rameez Uddin Nayak
Lymphangioma are benign, slow-growing and rare lymphatic tumors, which may emerge at any location in the body with ovary being a very rare location. Axillary region and neck are the most common sites, while retroperitoneum and mesentery account for <1%. We present a case of a young female of 33 years who had symptomatic pelvic mass and was presented with a complaint of lower abdominal pain of six-month duration and weight loss. Investigation revealed an oval-shaped complex cystic density lesion in the right adnexal region, which was likely neoplastic...
February 2024: Curēus
https://read.qxmd.com/read/38525086/retroperitoneal-mixed-neuroendocrine-non-neuroendocrine-neoplasm-a-case-report-and-review-of-literature
#23
John Adi Ashindoitiang, Victor Ikechukwu Canice Nwagbara, Theophilus Ugbem Ipeh, Ben Chukwu, Henry Olaleye Obanife, Alfred Ottoh Eyong, Maurice Efana Asuquo
The existence of both neuroendocrine and non-neuroendocrine histology in variable proportion in a lesion has been described by the World Health Organisation (WHO) as mixed neuroendocrine and non-neuroendocrine neoplasm (MiNEN). The pathogenesis of this tumour remains controversial but molecular studies point towards a common monoclonal origin. Tumours are classified as functioning and nonfunctioning based on substances secreted. The nonfunctioning tumours may be discovered due to its local effect. Presented is a 66-year-old male with an intra-abdominal mass, underwent laparotomy and excision biopsy with transient right lower limb lymphoedema...
2024: Rare Tumors
https://read.qxmd.com/read/38516175/primary-retroperitoneal-cavernous-hemangioma-a-case-report-and-review-of-the-literature
#24
Yuki Matsui, Sho Okada, Yoshihiro Nakagami, Takashi Fukagai, Kazuhiro Matsuda, Takeshi Aoki
Retroperitoneal cavernous hemangioma, a rare vascular tumor, has only 30 PubMed cases. Preoperative diagnostic criteria are unclear and often present asymptomatically until complications such as rupture or compression arise. We present a 73-year-old with chronic abdominal pain and a giant retroperitoneal tumor. Computed tomography (CT) and magnetic resonance imaging (MRI) revealed an irregular space-occupying mass in the retroperitoneum, suggesting a retroperitoneal chronic expanding hematoma. Total surgical resection confirmed the diagnosis as retroperitoneal cavernous hemangioma...
May 2024: Urology Case Reports
https://read.qxmd.com/read/38511034/germ-cell-tumor-presenting-as-a-mesenteric-cyst-a-case-report-and-literature-review
#25
Sana Ahuja, Saba Naaz, Adil Aziz Khan, Sufian Zaheer
Mesenteric cysts, typically benign and asymptomatic, are incidental findings during abdominal investigations for nonspecific symptoms. Their origin is commonly in the mesentery of the small bowel, mesocolon, or retroperitoneum. This paper reports a rare case of a 22-year-old male with a mesenteric cyst presenting as a right lower abdominal mass. Ultrasonography revealed a heterogenous collection, leading to surgical excision. Histopathology unexpectedly revealed an extragonadal yolk sac tumor (YST) originating in the mesentery, a rarity often misdiagnosed as a cyst...
March 2024: Indian Journal of Surgical Oncology
https://read.qxmd.com/read/38500901/unraveling-the-clinicopathological-diversity-and-subtypes-of-rhabdomyosarcoma-a-study-from-a-tertiary-care-center
#26
JOURNAL ARTICLE
Harika Mandava, Inuganti Venkata Renuka, Sudhakar Ramamoorthy
Background and objective Rhabdomyosarcoma (RMS) is a rare and malignant mesenchymal tumor characterized by skeletal muscle differentiation. While it is a common soft tissue sarcoma in children, its incidence significantly decreases with advancing age, rendering it exceptionally rare in individuals aged more than 45 years. This study aimed to shed light on the clinicopathological diversity and subtypes of RMS, thereby providing a comprehensive overview for enabling diagnostic precision and therapeutic strategies in treating this infrequently encountered malignancy in adults...
February 2024: Curēus
https://read.qxmd.com/read/38492514/well-differentiated-liposarcomas-and-dedifferentiated-liposarcomas-systemic-treatment-options-for-two-sibling-neoplasms
#27
REVIEW
A Kyriazoglou, A Pagkali, I Kotsantis, P Economopoulou, M Kyrkasiadou, M Moutafi, N Gavrielatou, M Anastasiou, A Boulouta, A Pantazopoulos, M Giannakakou, A Digklia, A Psyrri
Well-differentiated liposarcomas (WDLPS) and dedifferentiated liposarcomas (DDLPS) account for 60 % of all liposarcomas, reflecting the heterogeneity of this type of sarcoma. Genetically, both types of liposarcomas are characterized by the amplification of MDM2 and CDK4 genes, which indicates an important molecular event with diagnostic and therapeutic relevance. In both localized WDLPS and DDLPS of the retroperitoneum and the extremities, between 25 % and 30 % of patients have local or distant recurrence, even when perioperatively treated, with clear margins present...
April 2024: Cancer Treatment Reviews
https://read.qxmd.com/read/38476885/erdheim%C3%A2-chester-disease-of-multisystem-involvement-with-delayed-diagnosis-a-case-report-and-literature-review
#28
Xiaotong Shi, Guangzhi Sun, Tongguan Li, Mengjiao Xu, Yixuan Liu, Zhankui Wang, Yanfeng Hou
Erdheim-Chester disease (ECD) is a rare tumor of histiocytic origin, characterized by foamy or lipid-laden histiocytes mixed or surrounded by fibrosis that infiltrate multiple organs. Misdiagnosis is common due to the diversity of clinical presentations. The present study reported a case of ECD with the involvements of bone, cardiac, aorta and retroperitoneum. The patient had no obvious clinical symptoms and no noteworthy foamy histiocytes or Touton giant cells were found on pathological examination, delaying the diagnosis...
April 2024: Experimental and Therapeutic Medicine
https://read.qxmd.com/read/38473350/sex-differences-in-cancer-incidence-rates-by-race-and-ethnicity-results-from-the-surveillance-epidemiology-and-end-results-seer-registry-2000-2019
#29
JOURNAL ARTICLE
Sararat Tosakoon, Wayne R Lawrence, Meredith S Shiels, Sarah S Jackson
Men have 2-3 times the rate of most non-sex-specific cancers compared to women, but whether this is due to differences in biological or environmental factors remains poorly understood. This study investigated sex differences in cancer incidence by race and ethnicity. Cancer incidence data from the Surveillance, Epidemiology, and End Result (SEER) program (2000-2019) were used to calculate male-to-female incidence rate ratios (MF IRRs) for each cancer site, stratified by race and ethnicity, and age-standardized to the 2000 U...
February 29, 2024: Cancers
https://read.qxmd.com/read/38473300/the-future-of-targeted-therapy-for-leiomyosarcoma
#30
REVIEW
Ryan A Denu, Amanda M Dann, Emily Z Keung, Michael S Nakazawa, Elise F Nassif Haddad
Leiomyosarcoma (LMS) is an aggressive subtype of soft tissue sarcoma that arises from smooth muscle cells, most commonly in the uterus and retroperitoneum. LMS is a heterogeneous disease with diverse clinical and molecular characteristics that have yet to be fully understood. Molecular profiling has uncovered possible targets amenable to treatment, though this has yet to translate into approved targeted therapies in LMS. This review will explore historic and recent findings from molecular profiling, highlight promising avenues of current investigation, and suggest possible future strategies to move toward the goal of molecularly matched treatment of LMS...
February 26, 2024: Cancers
https://read.qxmd.com/read/38471222/primary-giant-hydatid-cyst-of-the-retroperitoneum-diagnosis-and-therapeutic-approaches
#31
A Sebai, R Elaifia, S Atri, A Ben Mahmoud, A Haddad, J M Kacem
INTRODUCTION AND IMPORTANCE: Primary hydatid cyst of the retroperitoneum is an exceedingly rare manifestation of hydatid disease. Diagnosis proves challenging due to nonspecific symptoms, and the condition is typically not suspected when facing a retroperitoneal cystic mass, necessitating awareness among clinicians and surgeons, particularly in endemic regions. CASE PRESENTATION: A 45-year-old male with a three-month history of progressive abdominal enlargement and pain...
March 8, 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38464925/management-of-retroperitoneal-high-grade-serous-carcinoma-of-unknown-origin-a-case-report
#32
Wen-Lin Hsieh, Dah-Ching Ding
BACKGROUND: Retroperitoneal high-grade serous carcinoma (HGSC) of unknown origin is a sporadic tumor that can originate from ovarian cancer. Herein, we report the case of a woman with retroperitoneal HGSC of unknown origin and describe how she was diagnosed and treated. CASE SUMMARY: A 71-year-old female presented with the tumor marker CA125 elevated to 1041.9 U/mL upon a regular health examination. Computed tomography revealed retroperitoneal lymph node enlargement...
February 26, 2024: World Journal of Clinical Cases
https://read.qxmd.com/read/38462578/unusual-imaging-findings-associated-with-abdominal-pediatric-germ-cell-tumors
#33
JOURNAL ARTICLE
Marie-Helene Gagnon, Paul-Robert Derenoncourt, Sampanna Rayamahi, Susan Taylor, Ashishkumar K Parikh, Maria R Ponisio, Geetika Khanna
Germ cell tumors of childhood are tumors arising from germline cells in gonadal or extragonadal locations. Extragonadal germ cell tumors are characteristically located in the midline, arising intracranially or in the mediastinum, retroperitoneum, or pelvis. These tumors are generally easily diagnosed due to typical sites of origin, characteristic imaging findings, and laboratory markers. However, germ cell tumors can be associated with unusual clinical syndromes or imaging features that can perplex the radiologist...
March 11, 2024: Pediatric Radiology
https://read.qxmd.com/read/38461584/a-retroperitoneal-pseudomyxoma-of-the-appendix-a-case-report
#34
Souhaib Atri, Aifia Rany, Mahdi Hammami, Amine Sebai, Sarra Laabidi, Montassar Kacem
INTRODUCTION: Retroperitoneal pseudomyxoma (RP) is a rare condition characterized by mucinous tumor growth within the retroperitoneal space, commonly originating from the appendix or other abdominal organs. RP presents with non-specific symptoms such as abdominal pain, bloating, and weight loss, making accurate diagnosis challenging. Due to its rarity and symptom overlap with other conditions, RP requires careful management by a multidisciplinary healthcare team. CASE PRESENTATION: An 82-year-old female with a three-month history of abdominal pain and an abdominal mass underwent diagnostic imaging, revealing a retroperitoneal cystic mass...
March 8, 2024: International Journal of Surgery Case Reports
https://read.qxmd.com/read/38455783/adenocarcinoma-induced-sigmoid-colon-intussusception-and-postoperative-parastomal-evisceration-in-an-elderly-patient-a-case-report-and-literature-review
#35
Jaber Alfaifi, Adeline Germain
Intussusception in adults is less frequent than in children, and it is less commonly seen in the colon than in the intestines. This may be explained by the fixation of the colon to the retroperitoneum. We herein describe a case of sigmoid colon intussusception caused by a sigmoid colon adenocarcinoma. An 81-year-old man presented with abdominal pain and signs and symptoms of gastrointestinal obstruction. CT revealed a "target sign" with a mass in the sigmoid colon. We diagnosed the patient with colonic obstruction secondary to intussusception of the sigmoid colon and performed an emergency transverse colostomy...
February 2024: Curēus
https://read.qxmd.com/read/38449407/-a-case-of-left-upper-abdominal-evisceration-for-transverse-colon-cancer-with-multiple-organ-invasion
#36
JOURNAL ARTICLE
Masato Fujino, Masahiro Amano, Fumie Osuga, Masatoshi Yoshizawa, Akina Kuwahara, Satoaki Kimura, Shinichiro Usuki, Norihito Hosoi, Yukinobu Shuto, Kunihisa Miyazaki
The case is a 73-year-old woman. She visited primary care doctor for abdominal pain, vomiting, diarrhea, and melena that persisted for 2 weeks. She was referred to our department because she had an elevated inflammatory response and CT showed a mass in her left upper quadrant. Contrast-enhanced CT showed a tumorous lesion mainly in the splenic flexure of the transverse colon, involving the greater curvature of the stomach, the tail of the pancreas, and the hilus of the spleen, accompanied by abscess formation...
February 2024: Gan to Kagaku Ryoho. Cancer & Chemotherapy
https://read.qxmd.com/read/38444644/retroperitoneal-schwannoma-during-pregnancy-a-case-report-and-practice-based-overview
#37
Stefano Fruci, Anna Fagotti, Silvia Salvi, Pierpaolo Mattogno, Quintino Giorgio D'Alessandris, Federica Totaro Aprile, Antonia Carla Testa, Antonio Lanzone, Liverana Lauretti
The retroperitoneum is the rarest site for Schwannomas, tumors that originate from Schwann cells and usually present as benign, slowly growing masses. During pregnancy, the routine application of ultrasound for fetal assessment has led to an increased rate of detection of maternal asymptomatic masses, notably including the retroperitoneal ones. While most of these masses prove to be benign, it is imperative to consider the potential for malignancy. This report presents a rare case involving a woman diagnosed with bilateral adnexal cysts and a pre-sacral retroperitoneal mass during the first trimester of pregnancy...
March 2024: Case Reports in Women's Health
https://read.qxmd.com/read/38429596/laparoscopic-necrosectomy-for-acute-necrotizing-pancreatitis-mesocolon-preserving-approach-and-outcomes
#38
JOURNAL ARTICLE
Yuxin Yang, Yang Liu, Zhiqiang Liu, Tao Peng, Chunyou Wang, Heshui Wu, Shanmiao Gou
The surgical treatment of acute necrotizing pancreatitis has significantly evolved in recent years with the advent of enhanced imaging techniques and minimally invasive surgery. Various minimally invasive techniques, such as video-assisted retroperitoneal debridement (VARD) and endoscopic transmural necrosectomy (ETN), have been employed in the management of acute necrotizing pancreatitis and are often part of step-up approaches. However, almost all reported step-up approaches only employ a fixed minimally invasive technique prior to open surgery...
March 1, 2024: Updates in Surgery
https://read.qxmd.com/read/38427760/disseminated-multiloculated-peritoneal-inclusion-cysts-bubble-trouble-in-belly
#39
JOURNAL ARTICLE
Md A Osama, Aditi Aggarwal, Seema Rao, Amitabh Yadav, Ritu Verma
Multiloculated peritoneal inclusion cysts, usually arise from peritoneal mesothelium lining the serous cavity of the abdomen, pelvis and retroperitoneum. These lesions can be incidentally found on imaging or during surgery, and confirmation of the diagnosis is done by radiological imaging, histomorphology and immunohistochemical findings. Although fewer than 200 cases of solitary peritoneal inclusion cysts have been reported, their occurrence in a disseminated fashion has hardly ever been described in literature...
February 19, 2024: Indian Journal of Pathology & Microbiology
https://read.qxmd.com/read/38425778/erdheim-chester-disease-with-tendon-and-muscle-involvement-reports-of-a-rare-presentation
#40
Mahshid Golagha, Fatemeh Dehghani Firouzabadi, Corina Millo, Moozhan Nikpanah, Mark A Ahlman, Rahul H Dave, Juvianee I Estrada-Veras, Kevin O'Brien, Ashkan A Malayeri
Erdheim-Chester disease (ECD) is a rare histiocytic disease that affects multiple systems in the body. While it typically targets long bones, cardiovascular structures, the retroperitoneum, and the central nervous system, reports of tendon and skeletal muscle involvement are scarce. This review presents 2 cases: a case of ECD involving the left Achilles tendon and left abductor hallucis, as well as an unusual manifestation of ECD in the thigh musculature. In Case 1, studies involved a 39-year-old man who initially presented with bone and pituitary involvement...
May 2024: Radiology Case Reports
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