Uterine carcinosarcomas are aggressive gynaecological cancers comprising less than 5% of uterine malignancies. We present the case of a woman in her 70s with a complicated history of advanced anal carcinoma treated with pelvic radiotherapy and multiple laparotomies, who was referred to gynae-oncology following MRI surveillance imaging showing evidence of endometrial carcinoma and para-aortic lymphadenopathy. Successful surgical excision required multidisciplinary teamwork between gynae-oncology, colorectal and urology surgeons. The patient underwent midline laparotomy, with adhesiolysis, ileum resection and side to side anastomosis, posterior exenteration, left kidney mobilisation and suspension, para-aortic lymph node debulking and left ureteric stent insertion. Significant challenge was posed by the extensive adhesions from previous laparotomies and the debulking of the para-aortic lymph nodes around the renal vessels. This case demonstrates the importance of a multidisciplinary approach in complex pelvic surgery and the vitality of good communication between colleagues in achieving effective patient care.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9716812PMC
http://dx.doi.org/10.1136/bcr-2022-252233DOI Listing

Publication Analysis

Top Keywords

para-aortic lymphadenopathy
8
anal carcinoma
8
para-aortic lymph
8
radical abdomino-pelvic
4
abdomino-pelvic surgery
4
surgery management
4
management uterine
4
uterine carcinosarcoma
4
carcinosarcoma concomitant
4
para-aortic
4

Similar Publications

Computed tomography findings of idiopathic multicentric Castleman disease subtypes.

J Clin Exp Hematop

December 2024

Department of Radiology, Faculty of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University, Okayama, Japan.

This study retrospectively evaluated the computed tomography (CT) findings of idiopathic multicentric Castleman disease (iMCD) at a single center and compared the CT findings of iMCD-TAFRO with those of iMCD-non-TAFRO. CT images obtained within 30 days before diagnostic confirmation were reviewed for 20 patients with iMCD (8 men and 12 women, mean age 52.8 ± 12.

View Article and Find Full Text PDF

The aim of the present study was to evaluate the occurrence of synchronous or metachronous hematologic and gynecologic malignancies. The medical database of the pathology department at a tertiary center was searched from 2016 to 2024 for cases involving both hematologic and gynecologic tumors. A literature search using Google Scholar and PubMed was also conducted between May and June 2024.

View Article and Find Full Text PDF

A 54-year-old woman with fever and cough presented with left upper lobe consolidation and para-aortic and hilar lymphadenopathies and was diagnosed with sarcoidosis, and her condition improved spontaneously. Over the next 15 years, the patient experienced seven similar episodes and was treated with glucocorticoids for the first time in the eighth episode, but subsequently died of respiratory failure. The autopsy revealed diffuse alveolar damage and co-infection with and Mucorales in the lungs and mediastinum.

View Article and Find Full Text PDF

Vanishing Bile Duct Syndrome: A Differential Diagnosis for Painless Jaundice.

Cureus

September 2024

Gastroenterology, Surrey and Sussex Healthcare NHS Trust, Redhill, GBR.

Article Synopsis
  • Vanishing bile duct syndrome (VBDS) is an acquired liver disease marked by the destruction of intrahepatic bile ducts, often linked to underlying conditions like Hodgkin's lymphoma.
  • The case presented involves a 69-year-old woman with symptoms including jaundice and fatigue, leading to a diagnosis of Hodgkin's lymphoma after further medical imaging.
  • Despite treatments such as steroids and chemotherapy, the patient ultimately passed away, underscoring the need for increased awareness and consideration of VBDS in diagnosing painless jaundice associated with cholestatic liver dysfunction.
View Article and Find Full Text PDF

Ewing sarcoma (ES) is a highly malignant and aggressive small round-cell tumor originating from primitive neuroepithelium and mesenchymal stem cells. It is usually seen in children and adolescents with a male predilection and a preponderance to occur in long bones. Although skeletal/soft tissue ES is encountered in clinical practice, primary ES of the genital tract, particularly bilateral primary ovarian ES, is highly uncommon, with only a handful of cases reported worldwide.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!