Advanced Ovarian Cancer with Splenic Infarct: A Case Report on Diagnostic Difficulties and Favorable Cytotoxic Effects

1981 ◽  
Vol 60 (5) ◽  
pp. 531-533
Author(s):  
Pertti Kirkinen ◽  
Antti Kauppila ◽  
Pentti Lohela
2021 ◽  
Vol 07 (02) ◽  
pp. e116-e120
Author(s):  
Tatjana Braun ◽  
Amelie De Gregorio ◽  
Lisa Baumann ◽  
Jochen Steinacker ◽  
Wolfgang Janni ◽  
...  

AbstractSplenosis is a rare disease, which is often discovered incidentally years after surgical procedures on the spleen or traumatic splenic lesions. Through injury of the splenic capsule, splenic cells are able to spread and autoimplant in a fashion similar to the process of metastatic cancer. Here we present the case of a 62-year-old female patient with a palpable tumor of the lower abdomen. Her medical history was unremarkable, except for splenectomy after traumatic splenic lesion in her childhood. Clinical examination and diagnostic imaging raised the suspicion of advanced ovarian cancer, which was further substantiated by the typical presentation of adnexal masses and disseminated peritoneal metastases during the following staging laparotomy. Surprisingly, we also found peritoneal implants macroscopically similar to splenic tissue. Microscopic examination of tissue specimens by intrasurgical frozen section confirmed the diagnosis of intra-abdominal splenosis. The patient then underwent cytoreductive surgery with complete resection of all cancer manifestations, sparing the remaining foci of splenosis to avoid further morbidity. This case demonstrates the rare coincidence of intra-abdominal carcinoma and splenosis, which could lead to intraoperative difficulties by misinterpreting benign splenic tissue. Therefore, splenosis should be considered in patients with medical history of splenic lesions and further diagnostic imaging like Tc-99m-tagged heat-damaged RBC scan could be used for presurgical distinguishing between tumor spread in the abdominal cavity and disseminated splenosis. The presented case report should not only raise awareness for the rare disease splenosis, but also emphasize the need to consider the possibility of simultaneous incidence of benign and malignant intra-abdominal lesions, as to our knowledge this is the first published case of simultaneous peritoneal carcinomatosis and splenosis.


2005 ◽  
Vol 97 (2) ◽  
pp. 693-696 ◽  
Author(s):  
Gabriella Ferrandina ◽  
Mariagrazia Distefano ◽  
Antonia Testa ◽  
Rosa De Vincenzo ◽  
Giovanni Scambia

2016 ◽  
Vol 37 (1) ◽  
pp. 129-130 ◽  
Author(s):  
Gee Hoon Lee ◽  
Mi Sun Kim ◽  
Min Chul Choi ◽  
Sang Geun Jung ◽  
Ah-Young Kwon ◽  
...  

Author(s):  
Sira Capote ◽  
José-Luis Sánchez-Iglesias ◽  
Montserrat Cubo-Abert ◽  
Javier De la Torre ◽  
Cristina Centeno-Mediavilla ◽  
...  

1996 ◽  
Vol 14 (7) ◽  
pp. 2101-2112 ◽  
Author(s):  
G Kemp ◽  
P Rose ◽  
J Lurain ◽  
M Berman ◽  
A Manetta ◽  
...  

PURPOSE Serious cumulative toxicity is a well-recognized consequence of chemotherapy. Amifostine, an organic thiophosphate, has demonstrated the ability to protect selectively a broad range of normal, but not neoplastic, tissues from the cytotoxic effects of chemotherapy and radiotherapy. This study was designed to determine if amifostine could reduce the serious toxicities associated with cyclophosphamide and cisplatin (CP), without reducing antitumor efficacy in patients with ovarian cancer. PATIENTS AND METHODS Two hundred forty-two patients with advanced ovarian cancer were randomized to receive six cycles of cyclophosphamide (1,000 mg/m2) and cisplatin (100 mg/m2) with or without amifostine (910 mg/m2) every 3 weeks for six cycles. The occurrence of hematologic, renal, neurologic, and ototoxicity was evaluated. Antitumor efficacy was assessed by pathologic tumor response and survival. RESULTS Pretreatment with amifostine before each cycle of chemotherapy resulted in a reduction of cumulative toxicities. Hematologic toxicity consisted of grade 4 neutropenia associated with fever and/or infection that required antibiotic therapy (P = .005), days in hospital (P = .019), and days on antibiotics (P = .031). Platinum-specific toxicities consisted of protracted serum creatinine elevations (P = 0.004), > or = 40% reduction from baseline in creatinine clearance (P = .001), and severity of neurologic toxicity (P = .029). Twenty-four percent of CP patients compared with 9% of amifostine plus CP patients discontinued therapy because of protocol-specified toxicity (P = .002). Pathologic tumor response rates were 37% with amifostine and 28% in controls, with comparable median survival times of 31 months. Amifostine was generally well tolerated; the principal side effects were emesis and a transient decrease in blood pressure. CONCLUSION Pretreatment with amifostine reduces the cumulative hematologic, renal, and neurologic toxicities associated with the CP regimen, with no reduction in antitumor efficacy.


Author(s):  
Sigit Purbadi ◽  
Junita Indarti ◽  
Hariyono Winarto ◽  
Andi Darma Putra ◽  
Kartiwa Hadi Nuryanto ◽  
...  

2006 ◽  
Vol 16 (Suppl 1) ◽  
pp. 391-393 ◽  
Author(s):  
G. Ostoros ◽  
A. Pretz ◽  
J. Fillinger ◽  
I. Soltesz ◽  
B. Dome

Fatal lung fibrosis caused by paclitaxel toxicity has not been reported In this report, we describe the case of a 62-year-old woman who received six cycles of paclitaxel and carboplatin as combination chemotherapy for advanced ovarian cancer. Four weeks after the end of the chemotherapy she developed interstitial pneumonitis and irreversible lung fibrosis. Despite treatment with corticosteroids, she had rapid deterioration and died of respiratory failure. Pulmonary fibrosis is a complication of paclitaxel therapy that may occur despite treatments with corticosteroids. While reviewing the literature, we found few less severe pulmonary injuries after intravenous use of paclitaxel, but none of these cases had a fatal outcome. Physicians should keep in mind that taxanes such as paclitaxel have the potential to cause pneumonitis and lung fibrosis.


2019 ◽  
Vol 163 (3) ◽  
pp. 113-115
Author(s):  
E.A. Bogush ◽  
◽  
O.A. Malikhova ◽  
T.V. Belyaeva ◽  
V.Yu. Kirsanov ◽  
...  

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