scholarly journals Unusually large prostatic utricle cyst

1970 ◽  
Vol 7 (1) ◽  
pp. 73-75
Author(s):  
K Paudel ◽  
A Kumar
Keyword(s):  
Complete Resolution ◽  
Cystic Lesion ◽  
Cystic Mass ◽  
Resonance Imaging ◽  
Prostatic Utricle ◽  
Posterior Urethra ◽  
Posterior Sagittal Approach ◽  
Magnetic Resonance Imaging Mri ◽  
Prostatic Utricle Cyst

Prostatic utricle cyst is one of the uncommon conditions and only a few cases have been reported. We present a case of unusually large prostatic utricle cyst in a 13- year- old male. He presented with burning urination and post-void dribbling of urine. A cystic mass was felt on digital per rectal examination. Ultrasound pelvis revealed a well-defined midline cystic mass posterior to the urinary bladder. Subsequent magnetic resonance imaging (MRI) of the pelvis demonstrated fluid containing cystic lesion communicating with posterior urethra. Surgical resection of the cyst was performed through the posterior sagittal approach. Follow up of the patient after three months of operation, there was complete resolution of the symptoms. Key words: Prostatic utricle cyst, MRI, Ultrasound doi: 10.3126/kumj.v7i1.1770 Kathmandu University Medical Journal (2009), Vol. 7, No. 1, Issue 25, 73-75

scholarly journals Prostatic Utricle Cyst as the Most Likely Cause in a Case of Recurrent Episodes of Hematospermia

2017 ◽  
Vol 2017 ◽  
pp. 1-3 ◽  
Author(s):  
Grégoire Feutry ◽  
Thomas De Perrot ◽  
Gregory J. Wirth ◽  
Xavier Montet ◽  
Steve P. Martin
Keyword(s):  
High Field ◽  
Cystic Lesion ◽  
Transrectal Ultrasound ◽  
Resonance Imaging ◽  
Endorectal Coil ◽  
Prostatic Utricle ◽  
Virgin Male ◽  
Magnetic Resonance Imaging Mri ◽  
Prostatic Utricle Cyst ◽  
Prostatic Cyst

Hematospermia is a clinical symptom that raises anxiety in patients and has various causes, benign and malignant. We report a case of hematospermia for which appropriate multidisciplinary expertise favored a conservative management of a benign prostatic cyst, namely, a prostatic utricle cyst. A cystic lesion found by transrectal ultrasound in the context of hematospermia related to masturbation in a young virgin male patient was investigated with a high-field magnetic resonance imaging (MRI) and an endorectal coil. The association of high-field MRI and endorectal coil leads to high quality images.

scholarly journals Knowledge Based Approach in Differential Diagnosis of Intracranial Cysts -A Requisite to Avoid Unwarranted Interventions

2012 ◽  
Vol 2 (1) ◽  
pp. 35-38 ◽  
Author(s):  
A Verma ◽  
A Moiyadi ◽  
S Arya ◽  
R Jalali ◽  
H Menon ◽  
...  
Keyword(s):  
Myeloid Leukemia ◽  
Cystic Lesion ◽  
Chemotherapy Regimen ◽  
Present Report ◽  
Resonance Imaging ◽  
Knowledge Based ◽  
Patient Reported ◽  
Intracranial Cysts ◽  
Magnetic Resonance Imaging Mri

Neuroglial cyst is a rare abnormality that is usually asymptomatic and an incidental detection in imaging done for an unrelated cause. An emphasis on this message is the prime aim of the present report. We came across a patient being treated for chronic myeloid leukemia having vague neurological symptoms for which Magnetic Resonance Imaging (MRI) was done. No detectable cause explaining his symptomatology was noted on imaging. A cystic lesion was however noted in right frontal lobe which was labeled as a neuroglial cyst. No treatment was mandated as per discussion in the neuro-oncology working group of our centre. Follow up was advised to confirm the impression as an attempt to achieve a histological diagnosis would have been ethically not justified. The patient reported regularly for his chemotherapy regimen to the respective unit and was asymptomatic for the lesion till last follow up at six months. NJR I VOL 2 I ISSUE 1 35-38 Jan-June, 2012 DOI: http://dx.doi.org/10.3126/njr.v2i1.6978

scholarly journals The prostatic utricle cyst with huge calculus and hypospadias: A case report and a review of the literature

2015 ◽  
Vol 9 (5-6) ◽  
pp. 345 ◽  
Author(s):  
Weigang Wang ◽  
Yuantao Wang ◽  
Dezhun Zhu ◽  
Pengfei Yan ◽  
Biao Dong ◽  
...  
Keyword(s):  
Computed Tomography ◽  
Cystic Lesion ◽  
Low Density ◽  
Review Of The Literature ◽  
Prostatic Utricle ◽  
History Of ◽  
Posterior Urethra ◽  
Frequent Micturition ◽  
Prostatic Utricle Cyst ◽  
Penoscrotal Hypospadias

Prostatic utricle cysts with calculus and hypospadias are rare in clinical practice. According to our literature review, only few cases have been reported. Recently, we experienced a case of prostatic utricle cyst with huge calculus in a 25-year-old male patient. He had a history of left cryptorchidism and surgery for penoscrotal hypospadias in his infancy. He was referred for frequent micturition, urgency of urination, urine pain, terminal hematuria and dysuria. Computed tomography (CT) revealed a retrovesical cystic lesion of low density, in which a 5×5 cm calcification was shown. Retrograde urethrocystography showed a 5×5 cm high-density shadow in the posterior urethra. The cyst was incised by transperineal approach and the stone was clearly observed and removed. Urethral stricture repair was performed simultaneously. The patient recovered smoothly after operation.

scholarly journals Embolization of a life-threatening placenta increta hemorrhage with a four-month MRI follow-up

2017 ◽  
Vol 6 (9) ◽  
pp. 205846011772778
Author(s):  
Annika Bach ◽  
Anne Bartens ◽  
Gabriele Gossing ◽  
Bernhard Gebauer ◽  
Rolf W Günther ◽  
...  
Keyword(s):  
Complete Resolution ◽  
Uterine Artery Embolization ◽  
Uterine Artery ◽  
Placental Tissue ◽  
Resonance Imaging ◽  
Placenta Increta ◽  
Artery Embolization ◽  
Life Threatening ◽  
Magnetic Resonance Imaging Mri

A 29-year-old woman with partial placenta increta was treated by bilateral uterine artery embolization (UAE) for bleeding with hemorrhagic shock two months after delivery, resulting in permanent hemostasis. The patient underwent a total of three magnetic resonance imaging (MRI) examinations—before UAE and four days and four months after UAE. At four months, MRI showed a fully regenerated uterus with preserved perfusion and complete resolution of residual placental tissue.

Magnetic Resonance Imaging (MRI) Diagnosis of Fetal Corpus Callosum Abnormalities and Follow-up Analysis

2021 ◽  
pp. 088307382110162
Author(s):  
Xu Li ◽  
Qing Wang
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
Corpus Callosum ◽  
Resonance Imaging ◽  
Neurodevelopmental Delay ◽  
Mri Diagnosis ◽  
Magnetic Resonance Imaging Mri ◽  
Lost To Follow Up ◽  
Singleton Pregnancies

Objectives: We analyzed the magnetic resonance imaging (MRI) manifestations of fetal corpus callosum abnormalities and discussed their prognosis based on the results of postnatal follow up. Methods: One hundred fifty-five fetuses were diagnosed with corpus callosum abnormalities by MRI at our hospital from 2004 to 2019. Gesell Development Scales were used to evaluate the prognosis of corpus callosum abnormalities after birth. Results: Corpus callosum abnormalities were diagnosed in 149 fetuses from singleton pregnancies, and 6 pairs of twins, 1 in each pair is a corpus callosum abnormality. Twenty-seven cases (27/155) were lost to follow up, whereas 128 cases (128/155) were followed up. Of these, 101 cases were induced for labor, whereas 27 cases were born naturally. Among the 27 cases of corpus callosum abnormality after birth, 22 cases were from singleton pregnancies (22/27). Moreover, 1 twin from each of 5 pairs of twins (5/27) demonstrated corpus callosum abnormalities. The average Gesell Development Scale score was 87.1 in 19 cases of agenesis of the corpus callosum and 74.9 in 3 cases of hypoplasia of the corpus callosum. Among the 5 affected twins, 2 had severe neurodevelopmental delay, 2 had mild neurodevelopmental delay, and 1 was premature and died. Conclusion: The overall prognosis of agenesis of the corpus callosum is good in singleton pregnancies. Hypoplasia of the corpus callosum is often observed with other abnormalities, and the development quotient of hypoplasia of the corpus callosum is lower compared with agenesis of the corpus callosum. Corpus callosum abnormalities may occur in one twin, in whom the risk may be increased.

scholarly journals Bone marrow abnormalities detected by magnetic resonance imaging as initial sign of hematologic malignancies

2018 ◽  
Author(s):  
Ida Sofie Grønningsæter ◽  
Aymen Bushra Ahmed ◽  
Nils Vetti ◽  
Silje Johansen ◽  
Øystein Bruserud ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Bone Marrow ◽  
Magnetic Resonance ◽  
Case Reports ◽  
Cell Types ◽  
Hematologic Malignancies ◽  
Resonance Imaging ◽  
Initial Sign ◽  
Magnetic Resonance Imaging Mri

The increasing use of radiological examination, especially magnetic resonance imaging (MRI), will probably increase the risk of unintended discovery of bone marrow abnormalities in patients where a hematologic disease would not be expected. In this paper we present four patients with different hematologic malignancies of nonplasma cell types. In all patients the MRI bone marrow abnormalities represent an initial presentation of the disease. These case reports illustrate the importance of a careful diagnostic follow-up without delay of patients with MRI bone marrow abnormalities, because such abnormalities can represent the first sign of both acute promyelocytic leukemia as well as other variants of acute leukemia.

scholarly journals Multifocal Balo's Concentric Sclerosis in Children: Report of a Case and Review of Literature

2017 ◽  
Vol 08 (S 01) ◽  
pp. S136-S138
Author(s):  
Sanjeev Kumar Bhoi ◽  
Suprava Naik ◽  
Jayantee Kalita ◽  
U. K. Misra
Keyword(s):  
Magnetic Resonance Imaging ◽  
Multiple Sclerosis ◽  
Acute Disseminated Encephalomyelitis ◽  
Review Of Literature ◽  
Resonance Imaging ◽  
Concentric Pattern ◽  
Baló’S Concentric Sclerosis ◽  
Magnetic Resonance Imaging Mri ◽  
Post Infectious

ABSTRACTBalo's concentric sclerosis (BCS) is a rare demyelinating lesion considered to be a variant of multiple sclerosis (MS). On magnetic resonance imaging (MRI) Balo's concentric sclerosis shows the typical concentric pattern. We report a case of 10 year old child with BCS who presented as post infectious acute disseminated encephalomyelitis (ADEM). He is asymptomatic and had no relapse after 6 years of follow-up.

scholarly journals Short-lasting unilateral neuralgiform headache with autonomic symptoms associated with idiopathic hypertrophic pachymeningitis

2018 ◽  
Vol 1 ◽  
pp. 251581631879054
Author(s):  
J Matthijs Biesbroek ◽  
Dirk R Rutgers ◽  
Sander van Gulik ◽  
Catherina JM Frijns
Keyword(s):  
Brain Mri ◽  
Resonance Imaging ◽  
Hypertrophic Pachymeningitis ◽  
Trigeminal Autonomic Cephalalgia ◽  
Autonomic Symptoms ◽  
Meningeal Inflammation ◽  
Magnetic Resonance Imaging Mri ◽  
Multiple Episodes ◽  
Rule Out

Short-lasting unilateral neuralgiform headache with autonomic symptoms (SUNA) is a rare form of trigeminal autonomic cephalalgia. SUNA is frequently associated with a trigeminal neurovascular conflict and rarely occurs secondary to other intracranial pathology. We report a patient with SUNA that was associated with ipsilateral meningeal inflammation caused by idiopathic hypertrophic pachymeningitis (HP). During the 9-year follow-up, she experienced multiple episodes of SUNA, most of which occurred during exacerbations of the pachymeningitis. This is the third case of SUNA associated with HP reported in the literature. Based on this observation, we suggest that in patients presenting with SUNA, besides dedicated magnetic resonance imaging (MRI) of the trigeminal nerve, gadolinium-enhanced brain MRI should be performed to rule out HP.

scholarly journals A midline prepontine cyst: Serial magnetic resonance imaging over 20 years shows very slow growth after its rapid shrinkage

2019 ◽  
Vol 32 (2) ◽  
pp. 98-102 ◽  
Author(s):  
Jun Sugata ◽  
Tessei Ueda ◽  
Natsuko Tanoue ◽  
Kazuho Hirahara ◽  
Kiyohisa Kamimura ◽  
...  
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
Slow Growth ◽  
Ventral Surface ◽  
Cystic Mass ◽  
Resonance Imaging ◽  
Weighted Magnetic Resonance Imaging ◽  
Rare Report ◽  
Pontomedullary Junction

An otherwise healthy 22-month-old boy suffered high fever, irritability, nausea, dysphagia, dysarthria and right hemiparesis. Magnetic resonance imaging showed a cystic mass, 15 mm in diameter, with surrounding oedema in the base of the lower pons. The symptoms subsided in about 10 days after onset, followed by a rapid decrease of the cyst size to 5 mm. Thereafter, the patient’s psychomotor growth has been normal. Annual follow-up magnetic resonance imaging scans showed very gradual enlargement of the cyst located on the ventral surface of the pontomedullary junction, reaching 16 mm in diameter in 21 years after onset. It was hyperintense on T1-weighted and isointense on T2-weighted magnetic resonance imaging. No haemosiderin deposition or gadolinium enhancement was seen. This is a rare report of a two decade longitudinal follow-up of a midline prepontine cyst showing asymptomatic and very slow growth. The possible nature of the cyst includes neurenteric, dermoid and epidermoid cyst.

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