scholarly journals A Rare Case of a Huge Retroperitoneal Tuberculous Cystic Mass in an 18 Year Old Ethiopian Female

2022 ◽  
pp. 55-58
Author(s):  
Dr Nasib Al Shibli
Keyword(s):  
Rare Case ◽  
Cystic Mass

scholarly journals A Rare Case of Functional Ectopic Hyperthyroidism: Struma Ovarii

2016 ◽  
Vol 8 (3) ◽  
pp. 212-213
Author(s):  
Indu Lata ◽  
Deepa Kapoor
Keyword(s):  
Rare Case ◽  
Histopathological Examination ◽  
Thyroid Tissue ◽  
Signs And Symptoms ◽  
Total Abdominal Hysterectomy ◽  
Abdominal Hysterectomy ◽  
Cystic Mass ◽  
Surgical Removal ◽  
Struma Ovarii ◽  
Lower Abdomen

ABSTRACT Struma ovarii (SO) is a rare special type of monodermal teratoma of ovary that predominantly consists of thyroid tissue (> 50%). In only 5 to 20% of cases hyperthyroidism is seen due to functional SO. We are reporting here a case of unilateral benign cystic SO in a 50-year-old postmenopausal lady presented with pain and heaviness in lower abdomen without any signs and symptoms of hyperthyroidism. Pelvic ultrasonogram showed right side tubo-ovarian mass and was planned for laparotomy. In preoperative investigation subclinical hyperthyroidism was diagnosed. Abdominal exploration showed cystic mass lesion in right ovary. She underwent total abdominal hysterectomy with bilateral salpingo-oophorectomy. Histopathological examination diagnosed the mass as benign cystic SO. Patient became euthyroid after surgical removal of tumor. How to cite this article Lata I, Kapoor D. A Rare Case of Functional Ectopic Hyperthyroidism: Struma Ovarii. World J Endoc Surg 2016;8(3):212-213.

scholarly journals Giant prostatic utricle with reflux mimicking ureteric diverticulum in the setting of a penoscrotal hypospadias: a rare case report

2019 ◽  
Vol 6 (11) ◽  
pp. 4187
Author(s):  
Amit Kumar ◽  
Rashi . ◽  
Amit Kumar Sinha ◽  
Bindey Kumar ◽  
Sambedna .
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Undescended Testis ◽  
Cystic Mass ◽  
Proximal Hypospadias ◽  
Prostatic Utricle ◽  
Rare Case Report ◽  
Penoscrotal Hypospadias

Prostatic utricle may present as big cystic mass and may mimic ureteral diverticulum. A giant prostatic utricle may be asymptomatic with proximal hypospadias with undescended testis. We are describing a case which was operated twice for hypospadias and then came to us with recurrent penoscrotal hypospadias. On workup giant prostatic utricle was diagnosed and managed.

scholarly journals Adult-onset giant cervical cystic hygroma with pressure manifestations on aerodigestive tract, managed surgically: reporting of a rare case

2019 ◽  
Vol 101 (3) ◽  
pp. e84-e87 ◽  
Author(s):  
Khaled Elshaar ◽  
Laila AbuAleid
Keyword(s):  
Computed Tomography ◽  
Rare Case ◽  
Lymphatic System ◽  
Paraffin Section ◽  
Cystic Hygroma ◽  
Cystic Mass ◽  
Adult Onset ◽  
Neck Swelling ◽  
Phrenic Nerves ◽  
Progressive Dysphagia

Cystic hygroma is a benign congenital malformation of the lymphatic system that occurs in children younger than two years of age. Hygroma commonly presents in head and neck but can be present anywhere. It is rarely seen in adults. We report the case of a 28-year-old woman who presented with a huge painless right-sided cystic neck swelling of 11 months duration, associated with progressive dysphagia and difficulty in breathing when lying supine or on her left side. Clinically, the swelling occupied both right anterior and posterior triangles of her neck with impalpable right carotid pulsations. Computed tomography revealed a cystic mass lesion. The mass was excised totally through right supraclavicular incision, after identification of the great auricular, spinal accessory and phrenic nerves. Paraffin section confirmed the diagnosis of cystic hygroma. After an uneventful postoperative period the patient was discharged and has had no recurrence to date.

scholarly journals Ovarian Adenomatoid Tumor Coexisting with Mature Cystic Teratoma: A Rare Case Report

2017 ◽  
Vol 2017 ◽  
pp. 1-3 ◽  
Author(s):  
Mingxia Shi ◽  
Firas Al-Delfi ◽  
Majd Al Shaarani ◽  
Kurt Knowles ◽  
James Cotelingam
Keyword(s):  
Rare Case ◽  
Cystic Teratoma ◽  
Cystic Mass ◽  
Mature Cystic Teratoma ◽  
Pathological Examination ◽  
Adenomatoid Tumor ◽  
Collision Tumors ◽  
Ultrasound Evaluation ◽  
Rare Case Report ◽  
The Right

Adenomatoid tumor of the ovary is rare, and so are collision tumors in this location. The most common histological combination of ovarian collision tumors is the coexistence of mature cystic teratoma with ovarian cystadenoma or cystadenocarcinoma. Presented herein is a rare case of ovarian adenomatoid tumor found incidentally and coexisting with mature cystic teratoma. A 44-year-old woman presented with a one-year history of intermittent right-sided pelvic pain. Ultrasound evaluation revealed a heterogeneous cystic mass in the right ovary, and a clinical diagnosis of teratoma was made. The patient subsequently underwent a right salpingo-oophorectomy. Pathological examination revealed a mature cystic teratoma and coexistent adenomatoid tumor. The two tumors were separate and no transitional features were recognized histologically. To our knowledge, no previous report of coexistence of these two tumors has been reported. Both tumors are benign and completely excised; therefore no adverse consequences are expected.

scholarly journals Lymphoepithelial Cyst in the Palatine Tonsil

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Fatih Bingöl ◽  
Hilal Balta ◽  
Buket Özel Bingöl ◽  
Recai Muhammet Mazlumoğlu ◽  
Korhan Kılıç
Keyword(s):  
Magnetic Resonance Imaging ◽  
Rare Case ◽  
Histopathological Examination ◽  
Cystic Mass ◽  
Palatine Tonsil ◽  
Lateral Part ◽  
Lymphoepithelial Cyst ◽  
Resonance Imaging ◽  
Tonsil Surgery ◽  
The Right

Lymphoepithelial cyst (LEC) is the most commonly encountered congenital neck pathology in the lateral part of the neck. A 66-year-old woman presented to the ENT clinic due to difficulty in swallowing persisting for approximately 1 year. Magnetic resonance imaging revealed a cystic mass at right tonsil. Surgery was performed due to this unilateral tonsillar mass, which was excised together with the right tonsil. LEC was diagnosed at histopathological examination. LEC in the palatine tonsil is rare, and only a few cases have been reported in the literature. We report a rare case of LEC in the palatine tonsil.

LARGE HYDATID CYST IN THIGH: A RARE CASE WITH CLINICO-RADIO-PATHOLOGICAL PROFILE

2010 ◽  
Vol 13 (03) ◽  
pp. 153-157 ◽  
Author(s):  
Inder Pawar ◽  
Amit Mittal ◽  
Permeet Bugga ◽  
Amit Aggarwal
Keyword(s):  
Differential Diagnosis ◽  
Hydatid Cyst ◽  
Female Patient ◽  
Rare Case ◽  
Cystic Mass ◽  
Left Thigh ◽  
Anatomic Location

We are presenting the case of a 26-year-old female patient who presented with a large swelling in the left thigh anteromedially. She was preoperatively diagnosed as a case of intramuscular hydatid cyst radiologically, and then cyst was removed and pathology proved the diagnosis. This case illustrates that echinococcal disease should be considered in the differential diagnosis of every cystic mass in any anatomic location, especially when they occur in areas where the disease is endemic.

scholarly journals Echocardiographic Manifestation of Esophagitis Mimicking a Posterior Mediastinal Mass

2014 ◽  
Vol 8s4 ◽  
pp. CMC.S18767
Author(s):  
Supreeya Swarup ◽  
Sowmya Kantamneni ◽  
Sarah Kabir ◽  
Roman Zeltser ◽  
Amgad N. Makaryus
Keyword(s):  
Computed Tomography ◽  
Rare Case ◽  
Patient Management ◽  
Mediastinal Mass ◽  
Posterior Mediastinum ◽  
Cystic Mass ◽  
Alter Patient ◽  
Posterior Mediastinal Mass ◽  
Posterior Mediastinal ◽  
Magnetic Resonance Scanning

Incidental extracardiac findings (ECFs) are commonly noted on cardiac imaging. The majority of the ECFs are noticed on computed tomography (CT), cardiac magnetic resonance scanning, and myocardial perfusion imaging. Although transthoracic echocardiography (TTE) is a widely used cardiac modality, there is scarcity of data describing ECF on TTE. ECFs have the potential to alter patient management. We present a rare case of a cystic mass seen in the posterior mediastinum on TTE, which led to further evaluation and diagnosis of esophagitis with ulceration.

scholarly journals A Rare Case of Craniopharyngioma in the Temporal Lobe

2017 ◽  
Vol 2017 ◽  
pp. 1-3
Author(s):  
Sasan Razmjoo ◽  
Seyed Nematollah Jazayeri ◽  
Mohammad Bahadoram ◽  
Maedeh Barahman
Keyword(s):  
Head Trauma ◽  
Temporal Lobe ◽  
Rare Case ◽  
Cystic Mass ◽  
Prior History ◽  
Mr Images ◽  
Left Temporal Lobe ◽  
History Of

Herein, we report on a rare case of craniopharyngioma arising in the left temporal lobe with no prior history of head trauma or surgery. There was a solid-cystic mass in the left temporal lobe on MR images. To the best of our knowledge, this is the second case of a craniopharyngioma occurring in the temporal lobe.

scholarly journals A rare case of retroperitoneal lymphangioma in a 74-year-old Chinese male

2021 ◽  
Vol 2021 (2) ◽  
Author(s):  
Hui Jun Lim ◽  
Joey Wee-Shan Tan ◽  
Claramae Shulyn Chia ◽  
Chin-Ann Johnny Ong
Keyword(s):  
Rare Case ◽  
Iliac Fossa ◽  
Cystic Mass ◽  
Left Iliac Fossa ◽  
Surgical Exploration ◽  
History Of ◽  
Retroperitoneal Lymphangioma ◽  
Chinese Male ◽  
Tomography Scan ◽  
Firm Mass

Abstract Retroperitoneal lymphangioma is an uncommon and benign mesodermal tumour that arises from the retroperitoneal lymphatics. Notably, it is a rare occurrence in adults, where <200 adult retroperitoneal lymphangioma cases have been published in the literature. Additionally, retroperitoneal lymphangioma is often difficult to diagnose preoperatively and formal diagnosis is frequently determined following surgical exploration. Here, we describe a rare case of retroperitoneal lymphangioma in a 74-year-old man who presented with a 6-month history of intermittent fresh per rectal bleeding with an incidental non-tender left iliac fossa firm mass on examination. Computed tomography scan established a retroperitoneal cystic lesion abutting the aorta and left common iliac vessels. Surgical exploration revealed a large cystic mass and a clean plane of dissection was performed, where the mass was completely excised with all the key structures preserved. Histology was consistent with a retroperitoneal lymphangioma.

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