scholarly journals Ultrasound Diagnostics of the Kidney Carbuncle (Brief Literature Review and Case Report of the Girl 5 Years Old)

2021 ◽  
pp. 150-160
Author(s):  
E. V. Dmitriyeva ◽  
M. N. Bulanov ◽  
V. E. Lykov ◽  
T. V. Barhatova
Keyword(s):  
Case Report ◽  
Kidney Disease ◽  
Literature Review ◽  
Rare Variant ◽  
Clinical Diagnostics ◽  
Review Of The Literature ◽  
Clinical Recovery ◽  
Ultrasound Diagnostics ◽  
Radiation Research ◽  
Illustrative Material

The article presents a case of preoperative diagnostics of a rare variant purulent-inflammatory kidney disease in children – the kidney carbuncle. The rarity of the pathology and the early child’s age (5 years old) determined complexity of clinical diagnostics and the importance of radiation research methods. The diagnosis was suspected by ultrasound diagnostics and confirmed by CT. The child was operated on (resection of the upper pole of the kidney), and clinical recovery was achieved. The article includes illustrative material and a brief review of the literature on this problem.

Familial Eruptive Syringomas: Case Report and Review of the Literature

2013 ◽  
Vol 17 (2) ◽  
pp. 84-88 ◽  
Author(s):  
Jenny Lau ◽  
Richard M. Haber
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Clinical Entity ◽  
Benign Neoplasms ◽  
Review Of The Literature ◽  
Causative Gene ◽  
Unusual Condition ◽  
Clinical Variant ◽  
Insight Into

Background: Syringomas are benign neoplasms of eccrine origin. A clinical variant is eruptive syringomas, which presents as firm, smooth, yellow to pigmented papules that appear as successive crops on the neck, axillae, chest, abdomen, and/or periumbilical region. To our knowledge, there are only 10 published reports of familial eruptive syringomas. Herein we describe the eleventh report of familial eruptive syringomas, review the literature on this unusual presentation, and suggest a novel classification of familial syringomas based on our literature review. Observations: We report two cases of eruptive syringoma within a family. Eruptive syringomas were widely distributed on the trunk of a healthy 16-year-old female and her 19-year-old brother. Both the 19-year-old man and his mother also had infraorbital syringomas. Conclusion: Familial eruptive syringomas are a rare clinical entity that is likely autosomal dominantly inherited. Future reports of this unusual condition may provide further insight into the etiology of familial syringomas, and genetic analysis of cases may enable the causative gene mutation to be determined.

scholarly journals Nocardiosis in Kidney Disease Patients under Immunosuppressive Therapy: Case Report and Literature Review

2019 ◽  
Vol 16 (6) ◽  
pp. 838-844 ◽  
Author(s):  
Tao Wang ◽  
Yun Jia ◽  
Bao Chu ◽  
HongTao Liu ◽  
XiaoLi Dong ◽  
...  
Keyword(s):  
Case Report ◽  
Kidney Disease ◽  
Literature Review ◽  
Immunosuppressive Therapy

Tremor Caused by Dandy-Walker Syndrome Concomitant with Syringomyelia: Case Report and Review of the Literature Review

2020 ◽  
Vol 136 ◽  
pp. 301-304
Author(s):  
Yiqi Wang ◽  
Shunyuan Guo ◽  
Liang'e Xu ◽  
Yu Geng ◽  
Zongjie Shi ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Review Of The Literature

scholarly journals A case report and review of the literature of Bouveret syndrome

2020 ◽  
Vol 102 (1) ◽  
pp. e15-e19 ◽  
Author(s):  
G Singh ◽  
N Merali ◽  
S Shirol ◽  
P Drymousis ◽  
S Singh ◽  
...  
Keyword(s):  
Case Report ◽  
Surgical Treatment ◽  
Rare Variant ◽  
Gastric Outlet Obstruction ◽  
Gallstone Ileus ◽  
Outlet Obstruction ◽  
Review Of The Literature ◽  
First Case ◽  
Bouveret Syndrome

Bouveret syndrome is a rare variant of gallstone ileus causing gastric outlet obstruction. It results from the formation of either a cholecystoduodenal or a cholecystogastric fistula and subsequent migration of gallstone into the duodenum or pylorus of stomach, causing obstruction. The first case was reported by Leon Bouveret in 1896. We report a case illustrating the rarity and severity of this condition, together with a review of the literature of the different methods of endoscopic and surgical treatment.

A rare variant of acinic cell carcinoma of the upper lip: A case report and review of the literature

1990 ◽  
Vol 69 (1) ◽  
pp. 84-88 ◽  
Author(s):  
Shigeo Eda ◽  
Hiromasa Hasegawa ◽  
Chihito Nakamura ◽  
Tadashi Yamazaki ◽  
Toshiyuki Kawakami
Keyword(s):  
Case Report ◽  
Cell Carcinoma ◽  
Rare Variant ◽  
Acinic Cell Carcinoma ◽  
Review Of The Literature ◽  
Upper Lip ◽  
Acinic Cell

RARE VARIANT OF TOTAL ANOMALOUS PULMONARY VENOUS CONNECTION: Intrapulmonary Drainage of One Lung by the Other- A Case Report and Review of the Literature

1997 ◽  
Vol 17 (1) ◽  
pp. 133-140
Author(s):  
Jin Haeng Chung ◽  
Yeon-Lim Suh ◽  
Heung Jae Lee ◽  
I-Seok Kang ◽  
Yeon Hyeon Choe ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Variant ◽  
The Other ◽  
Review Of The Literature ◽  
Anomalous Pulmonary Venous Connection

scholarly journals Sphenoid Wing Meningioma Presenting as Sudden Sensorineural Hearing Loss: A Case Report and Literature Review

2020 ◽  
pp. 014556132090573
Author(s):  
Edgar del Toro ◽  
Adwight Risbud ◽  
Nima Khosravani ◽  
Gennadiy Vengerovich ◽  
Alfredo Archilla
Keyword(s):  
Hearing Loss ◽  
Case Report ◽  
Literature Review ◽  
Sensorineural Hearing Loss ◽  
Unusual Case ◽  
Sudden Sensorineural Hearing Loss ◽  
Sensorineural Hearing ◽  
Review Of The Literature ◽  
Unusual Symptoms ◽  
Sphenoid Wing Meningioma

Sphenoid wing meningiomas are tumors that typically present with vision deterioration and neurological changes due to their proximity to the sella, cavernous sinus, and other vital structures. Some unusual symptoms have also been described in the literature, such as cognitive dysfunction, parkinsonism, and intracerebral hemorrhage. In this report, we detail another unusual case of sphenoid wing meningioma in a 63-year-old female who presented with left sudden sensorineural hearing loss. A brief review of the literature is also included.

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