asymptomatic woman
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2021 ◽  
Author(s):  
Neha Khaitan ◽  
Christine N. Booth ◽  
Raza S. Hoda
Keyword(s):  
Pap Test ◽  

2021 ◽  
Vol Publish Ahead of Print ◽  
Author(s):  
Maria Brambati ◽  
Enrico Borrelli ◽  
Francesco Trevisani ◽  
Elena Bruschi ◽  
Francesco Bandello ◽  
...  

2021 ◽  
Vol 14 (1) ◽  
pp. e235421
Author(s):  
Hannah Thorman ◽  
Nikita R Bhatt ◽  
Sona Kapoor ◽  
Azad Hawizy

A 62-year-old asymptomatic woman with diabetes was referred to the urology department from nephrology due to deterioration in renal function with accompanied right-sided hydronephrosis on ultrasound. CT imaging subsequently revealed a right-sided staghorn calculus and a significant volume of gas in the right collecting system from the kidney to the distal ureter, in keeping with emphysematous pyelitis. She was admitted and managed with antibiotics and insertion of right nephrostomy in the first instance, followed by percutaneous nephrolithotomy to definitively manage the stone. The patient remained asymptomatic throughout the process.


2020 ◽  
Vol 3 (2) ◽  
pp. 56-59
Author(s):  
Rojina Manandhar ◽  
Asha Singh ◽  
Abhimanyu Shrestha ◽  
Sebak Shrestha

Fitz-Hugh-Curtis syndrome (FCHS), also known as acute perihepatitis, is a rare disorder characterised by inflammation of the peritoneum and the tissues surrounding the liver. This syndrome can arise as a potential complication from a pelvic inflammatory disease caused by Neisseria gonorrhoeae or Chlamydia trachomatis. This is a case of 26 years’ healthy asymptomatic woman with primary infertility where this syndrome was diagnosed incidentally during laproscopy.


2020 ◽  
Vol 196 ◽  
pp. 127-129 ◽  
Author(s):  
Wynn Peterson ◽  
Zachary Liederman ◽  
Jillian Baker ◽  
Georgina Floros ◽  
Rachel Martin ◽  
...  

2020 ◽  
Vol 2020 ◽  
pp. 1-3
Author(s):  
Franco Pepe ◽  
Gianmarco Marchese ◽  
Gabriele Giuseppe Pepe ◽  
Elisabetta Zambrotta ◽  
Giulio Insalaco ◽  
...  

A 25-year-old woman presented to the obstetric clinic in her first pregnancy. The patient was accompanied by her mother who reported an episode of intracerebral hemorrhage after birth and also remembered access to the emergency department after generalized tonic-clonic seizure as an infant. She was not able to describe the therapy for seizure preventions and even when and why it was suspended, but she affirmed that no residual neurological consequences were detected in the following years. Actually, the pregnant woman was in good health without neurological symptoms nor assumed any therapy. A neurologist reviewed the patient’s CT scan in which arachnoid cyst and porencephalic cyst were evident, and he assessed that no abnormalities were found in motor, sensory, and mental state examination. EEG did not show any epileptiform or seizure-like activity. No antiepileptic drug was prescribed due to the absence of symptoms since many years. The patient had no neurological symptoms during pregnancy or obstetric complications and delivered at term a healthy baby through a caesarean section. She breastfed, and after two years, the patient and the baby are healthy. The association of porencephalic and arachnoid cyst in pregnancy is an extremely rare neurological condition that needs a multidisciplinary counseling in pregnancy, but an uneventful course is possible.


2020 ◽  
Vol 5 (1-2) ◽  
pp. 75-79
Author(s):  
Isabelle Fülber ◽  
Katharina Peer ◽  
Elisabeth Maurer ◽  
Detlef K. Bartsch ◽  
Jannis Görlach ◽  
...  

AbstractSchwannomas are benign tumors in 95% of cases and very rarely occur in the retroperitoneum. We report the cases of a 35-year-old man with abdominal discomfort and a 50-year-old asymptomatic woman with large retroperitoneal masses. Both underwent multivisceral surgery to exclude an adrenal carcinoma, and the pathologic diagnosis showed schwannomas in both cases. Despite morphological imaging, it was not possible to get a clear diagnosis preoperatively.


2020 ◽  
Vol 2020 ◽  
pp. 1-4
Author(s):  
Estella Musacchio ◽  
Andrea Piotto ◽  
Pierluigi Binotto ◽  
Antonio Toniato ◽  
Leonardo Sartori

Introduction. We report the resolution of tooth discoloration following parathyroidectomy in an otherwise asymptomatic woman with primary hyperparathyroidism-associated hypercalcemia. Case Report. A 59-year-old Caucasian woman, diagnosed with primary hyperparathyroidism in 2011, nonsmoker with excellent overall oral health. She complained of tooth discoloration starting in 2013. Pigmentation was particularly evident in the necks of the lower central and lateral incisors (Vita Classical score C2). No bleaching was undertaken. Parathyroidectomy was performed five years after primary hyperparathyroidism diagnosis. Six months later, a reduction in pigmentation was strikingly evident, with incisors scoring A1 and A2. The improvement persisted over time. Tooth value also increased compared to baseline. Conclusions. This is, to our knowledge, the first report that parathyroidectomy might resolve dental discoloration. This outcome deserves investigation in a meaningful sample size and may eventually prompt the inclusion of dental issues among the consequences of primary hyperparathyroidism.


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