scholarly journals Epididymal Leiomyosarcoma: One Case Report

2012 ◽  
Vol 2012 ◽  
pp. 1-2 ◽  
Author(s):  
Mohammed Fadl Tazi ◽  
Ahmed Amine Bouchikhi ◽  
Youness Ahallal ◽  
Soufiane Mellas ◽  
Jalaleddine Elammari ◽  
...  
Keyword(s):  
Case Report ◽  
Medical History ◽  
African Origin ◽  
History Of ◽  
Histological Confirmation

Epididymal leiomyosarcoma is very uncommon. Only 16 cases have been reported in the literature. There has never been a reported case of a patient with an African origin with this tumor. We report the medical history of a 70-year-old man who presented an enormous mass located in his epididymis. A tricut biopsy was performed which allowed histological confirmation of epididymal leiomyosarcoma after which the patient underwent excision of the mass. The patient died after the first round of chemotherapy.

Agranulocytosis Associated with Waldenström Macroglobulinemia

2018 ◽  
Vol 140 (1) ◽  
pp. 42-45 ◽  
Author(s):  
Iuliana Vaxman ◽  
Daniel Shepshelovich ◽  
Lucille Hayman ◽  
Pia Raanani ◽  
Meir Lahav
Keyword(s):  
Case Report ◽  
Febrile Neutropenia ◽  
Medical History ◽  
Case Reports ◽  
Neutropenic Fever ◽  
Severe Neutropenia ◽  
Past Medical History ◽  
Waldenström Macroglobulinemia ◽  
Waldenstrom Macroglobulinemia ◽  
History Of

Currently, there are only 2 case reports of Waldenström macroglobulinemia (WM) associated with severe neutropenia. This is a case report of a woman with a past medical history of WM who presented with neutropenic fever. The patient’s febrile neutropenia resolved after RCD chemotherapy (cyclophosphamide 750 mg/m2, dexamethasone 20 mg, and rituximab 375 mg/m2). Fourteen days after administration, the neutrophil level had started to rise and normalized after 6 days. To the best of our knowledge, this is the 3rd reported case of agranulocytosis due to WM.

scholarly journals Nicotine stomatitis in smokers: a case report

2018 ◽  
Vol 3 (1) ◽  
pp. 58
Author(s):  
Doni MS. Prabowo ◽  
Haris B. Widodo
Keyword(s):  
Case Report ◽  
Salivary Glands ◽  
Medical History ◽  
Smokeless Tobacco ◽  
Hard Palate ◽  
World Population ◽  
Minor Salivary Glands ◽  
White Spots ◽  
The World ◽  
History Of

Objective: The aim of this study is to describe and analyse nicotine stomatitis in smokers. Of the world population that consumes tobacco, Asia and Australia make up 57% of tobacco consumers. Tobacco can be consumed by various ways such as smoked tobacco, commonly known as cigarettes, or smokeless tobacco. Cigarettes are known to cause nicotine stomatitis in the oral cavity.Methods: A 28-year-old man patient came with complaints of white spots on his hard palate. The patient has a medical history of asthma as a child and has been taking salbutamol. The patient has been smoking 3 packs of cigarettes a day since being 16 years old.Results: Nicotine stomatitis that occurs on the hard palate appears as circular reddish shapes on the orifice of minor salivary glands. These lesions are formed from physically irritation caused by smoking. The lesions were benign and reversible.Conclusion: Thought appropriate examination and treatment, these lesions were healed.

scholarly journals Incidental detection of retained oil-based hysterosalpingography contrast medium with postoperative postpartum radiography: A case report

2021 ◽  
Author(s):  
Harue Hayashida ◽  
Kiichiro Furuya ◽  
Hiroki Kurahashi ◽  
Saya Yamashita ◽  
Yangshil Chang ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Caesarean Section ◽  
Contrast Medium ◽  
Medical History ◽  
Assisted Reproductive Technology ◽  
Reproductive Technology ◽  
Pelvic Cavity ◽  
History Of

Hysterosalpingography (HSG) is widely performed in combination with assisted reproductive technology, and the contrast medium used in this procedure may be retained in the pelvic cavity. In patients showing suspected operative-residue lesions after caesarean section, a medical history of HSG and details regarding abnormal findings can facilitate differential diagnosis.

Impaired Extension of the Digits due to Bilateral Idiopathic Intrinsic Contracture: A Case Report

2019 ◽  
Vol 24 (03) ◽  
pp. 383-385
Author(s):  
Yuki Kawasaki ◽  
Soichi Ejiri ◽  
Michiyuki Hakozaki ◽  
Shinichi Konno
Keyword(s):  
Eating Disorder ◽  
Case Report ◽  
Surgical Treatment ◽  
Conservative Treatment ◽  
Medical History ◽  
Rare Condition ◽  
Tendon Sheath ◽  
Past Medical History ◽  
Thenar Muscle ◽  
History Of

Idiopathic intrinsic contracture (IIC) with no history of trauma, ischemia, or spasticity is extremely rare. We report herein a case of impaired extension of the digits due to bilateral IICs occurred in a 30-year-old woman with a past medical history of eating disorder and amenorrhea. Although no previous case has been reported in the literature, eight similar cases of IIC have been presented at Japanese domestic conferences. In these eight cases and the present case, resection of the thenar muscle cords and unilateral resection of the lateral band were effective. Since IIC in patients with an eating disorder is a rare condition, it would be treated conservatively at first as tendon sheath inflammation or locking. However, this condition may be resistant to conservative treatment, and surgical treatment should be considered in such cases.

Proptosis of the eye: a potential form of Madelung’s disease

2021 ◽  
Vol 14 (9) ◽  
pp. e243669
Author(s):  
Shayan Soomro ◽  
Kimia Ziahosseini ◽  
Poonam Sharma
Keyword(s):  
Adipose Tissue ◽  
Case Report ◽  
Optic Nerve ◽  
Medical History ◽  
Madelung's Disease ◽  
Madelung’S Disease ◽  
Potential Form ◽  
History Of ◽  
The Stability ◽  
Genetic Form

Madelung’s disease is a rare disorder characterised by excessive and symmetrical deposits of adipose tissue, typically in the cervicofacial region. Alcohol is a known cause of the condition, however, there are reports that this condition is genetically inherited. Lipomatosis of the orbit has been described in the alcoholic Madelung’s disease, however, in our case report, we believe this is the first reported instance of proptosis caused by the genetic form of the condition. We present a 69-year-old woman, with a medical history of genetic Madelung’s disease, who presented with bilateral proptosis worse in her right eye. Her ocular examination was normal apart from exophthalmometry, showing bilateral proptosis. This was confirmed by an MRI, which further showed intraorbital fat deposition bilaterally. Due to the stability of her condition, no treatment was deemed necessary. We highlight the importance of monitoring for progressive optic nerve compromise and liposarcomatous malignant transformation.

scholarly journals Pregnancy-associated atypical haemolytic uraemic syndrome in the postpartum period: a case report and review of the literature

2011 ◽  
Vol 4 (2) ◽  
pp. 83-85 ◽  
Author(s):  
M Egbor ◽  
A Johnson ◽  
F Harris ◽  
D Makanjoula ◽  
H Shehata
Keyword(s):  
Case Report ◽  
Medical History ◽  
Postpartum Period ◽  
Haemolytic Uraemic Syndrome ◽  
Review Of The Literature ◽  
Atypical Haemolytic Uraemic Syndrome ◽  
History Of ◽  
Previous Medical History

Pregnancy has been reported to be a trigger in about 10% of all patients with atypical haemolytic uraemic syndrome (aHUS). However, in contrast to pregnancy-associated thrombotic thrombocytopaenic purpura, the presentation of pregnancy-associated aHUS remains ill defined and can therefore be difficult to diagnose and manage appropriately. Here we report a case of pregnancy-associated relapse of aHUS in a patient with a previous medical history of aHUS prior to pregnancy.

scholarly journals Human penile ossification: case report

2007 ◽  
Vol 125 (2) ◽  
pp. 124-125 ◽  
Author(s):  
Homero Oliveira de Arruda ◽  
Hudson de Lima ◽  
Valdemar Ortiz
Keyword(s):  
Case Report ◽  
Rare Condition ◽  
Penile Shaft ◽  
Palpable Mass ◽  
Slight Pain ◽  
History Of ◽  
One Year ◽  
Histological Confirmation ◽  
Metaplastic Bone ◽  
Firm Mass

CONTEXT: Ossification in the human penis is such a rare condition that only 34 histologically evident cases have previously been reported. Among several conditions that have been correlated with this problem the most frequent is Peyronie disease. In all these conditions, human penile ossification appears to be a metaplastic bone formation process. CASE REPORT: A 59-year-old white man presented with a one-year history of slight pain upon erection and during intercourse. He also complained of hard plaque near the base of the penis. One year earlier, he had sustained blunt trauma during intercourse. Examination of the penis revealed a fixed firm mass extending over the proximal third of the penile shaft, measuring 3.0 x 3.0 x 2.0 cm and involving the corporal sponge, without surface extension. There was no impotence or other relevant clinical finding. Radiography on the penis revealed irregular calcification in the same position as the palpable mass and in the septum of the proximal inner third of the penis. The importance of this report lies in the extent of the human penile ossification, as demonstrated by the radiological and histological confirmation.

scholarly journals A CASE REPORT ON WILSON'S DISEASE INDUCED LIVER CIRRHOSIS

2017 ◽  
Vol 10 (4) ◽  
pp. 113
Author(s):  
Remya Reghu ◽  
Bini Vincent ◽  
Aloysius James ◽  
Syamaprasad Tv ◽  
Reshma Reji
Keyword(s):  
Liver Cirrhosis ◽  
Case Report ◽  
Portal Hypertension ◽  
Medical History ◽  
Copper Deposit ◽  
Copper Transport ◽  
Medical Professionals ◽  
Genetic Abnormality ◽  
History Of ◽  
Cellular Copper

ABSTRACTWilsons disease is an inherited autosomal genetic abnormality genetic abnormality which results in impairment in cellular copper transport. Overtime this may leads to liver cirrhosis. The main focus of this case is to shows the importance of taking medical history. Here we discuss a case of 35 year old male diagnosed with Wilsons disease induced Liver cirrhosis and portal hypertension. He was physically very weak. Since the same genetic abnormality was the reason for the death of his sibling which was not considered while taking the medical history of this patient, this led to a late diagnosis of 4 years while the patient's condition became worst. Here in we report a case that provides an insight to medical professionals about taking proper medical history of patients.Key Words : Wilsons Disease, Liver Cirrhosis, Copper Deposit

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