scholarly journals Sacrum metastasis in carcinoma gall bladder: an unusual presentation

2020 ◽  
Vol 8 (5) ◽  
pp. 1884
Author(s):  
Sanjay Sajeevan ◽  
Biswajyoti Das ◽  
Yanpothung Yanthan ◽  
Naseef P. K. ◽  
Sweety Gupta ◽  
...  
Keyword(s):  
Bone Metastasis ◽  
Gall Bladder ◽  
Rare Case ◽  
Case Reports ◽  
Unusual Presentation ◽  
Skeletal Metastases ◽  
Common Site ◽  
Carcinoma Gall Bladder ◽  
Abdominal Metastasis ◽  
Time Of Presentation

Disseminated blood-borne metastases from carcinoma of the gall bladder are uncommon and usually occur late. The most common site of extra-abdominal metastasis is lung followed by brain. Skeletal metastases in carcinoma gall bladder are very rare. To date there have only been a few case reports of bone metastasis in carcinoma gall bladder at the time of presentation. Authors here present a rare case of carcinoma gall bladder that progressed to isolated sacrum metastasis. 

scholarly journals CARCINOMA GALL BLADDER-AN UNUSUAL PRESENTATION

1998 ◽  
Vol 54 (4) ◽  
pp. 347-348
Author(s):  
BM NAGPAL ◽  
RK BAJPAI ◽  
KJ SINGH ◽  
JS PANAYCH ◽  
KK MAUDAR
Keyword(s):  
Gall Bladder ◽  
Unusual Presentation ◽  
Carcinoma Gall Bladder

scholarly journals Occult hemoptysis: a rare case of esthesioneuroblastoma

2020 ◽  
Vol 6 (8) ◽  
pp. 1542
Author(s):  
Shalini Jain ◽  
Kanwer Sen
Keyword(s):  
Clinical Diagnosis ◽  
Rare Case ◽  
Systematic Approach ◽  
Case Reports ◽  
Signs And Symptoms ◽  
Clinical Suspicion ◽  
Unusual Presentation ◽  
Chest Physician ◽  
Chief Complaints ◽  
Nose And Throat

<p>Esthesioneuroblastoma forms a part of the spectrum of rare malignancies of the olfactory neuroepitheliem. The rarity of the tumour precludes systematic approach to clinical diagnosis and management. This study involves a case of 68 years old female who presents with chief complaints of hemoptysis for 3 months in the medical outpatient department with no nasal signs and symptoms. After referral to chest physician she is referred for ear nose and throat opinion. Esthesioneuroblastoma presentation is very varied and the case reports published have been very few. In view of the rarity of the tumour, clinical suspicion is essential in unusual presentation of hemoptysis.</p>

scholarly journals Case reports: mild COVID-19 infection and acute arterial thrombosis

2020 ◽  
Vol 2020 (9) ◽  
Author(s):  
Dixon Osilli ◽  
Jelena Pavlovica ◽  
Rashi Mane ◽  
Mohammed Ibrahim ◽  
Amina Bouhelal ◽  
...  
Keyword(s):  
Arterial Thrombosis ◽  
Respiratory Symptoms ◽  
Case Reports ◽  
Unusual Presentation ◽  
Initial Assessment ◽  
Time Of Presentation ◽  
Work Up

Abstract We present two cases of acute arterial thrombosis in patients who were confirmed to be SARS-CoV-2 positive. Neither of the patients had a background of underlying vascular morbidity. At the time of presentation, both patients exhibited only mild respiratory symptoms of COVID-19. After initial assessment and work-up, both patients underwent surgery for their respective vascular pathologies. They both did well post-operatively and were discharged home. This is an unusual presentation of acute arterial thrombosis in two patients with only mild symptoms of COVID-19 infection.

Herpetic Whitlow of the Hand in Infants

2020 ◽  
Author(s):  
Mohammad M. Al-Qattan ◽  
Nada G. AlQadri ◽  
Ghada AlHayaza
Keyword(s):  
Bacterial Infection ◽  
Case Reports ◽  
Case Series ◽  
Individual Case ◽  
Senior Author ◽  
Secondary Bacterial Infection ◽  
Clinical Appearance ◽  
History Of ◽  
Mode Of Transmission ◽  
Time Of Presentation

Abstract Introduction Herpetic whitlows in infants are rare. Previous authors only reported individual case reports. We present a case series of six infants. Materials and Methods This is a retrospective study of six cases of herpetic whitlows in infants seen by the senior author (MMA) over the past 23 years (1995–2017 inclusive). The following data were collected: age, sex, digit involved in the hand, mode of transmission, time of presentation to the author, clinical appearance, presence of secondary bacterial infection, presence of other lesions outside the hand, method of diagnosis, treatment, and outcome. Results All six infants initially presented with classic multiple vesicles of the digital pulp. In all cases, there was a history of active herpes labialis in the mother. Incision and drainage or deroofing of the vesicles (for diagnostic purposes) resulted in secondary bacterial infection. Conclusion The current report is the first series in the literature on herpetic whitlows in infants. We stress on the mode of transmission (from the mother) and establishing the diagnosis clinically. In these cases, no need for obtaining viral cultures or polymerase chain reaction; and no medications are required. Once the vesicles are disrupted, secondary bacterial infection is frequent and a combination of oral acyclovir and intravenous antibiotics will be required.

Linezolid Induced Skin Reactions in a Multi Drug Resistant Infective Endocarditis Patient: A Rare Case

2020 ◽  
Vol 15 (3) ◽  
pp. 222-226 ◽  
Author(s):  
Asha K. Rajan ◽  
Ananth Kashyap ◽  
Manik Chhabra ◽  
Muhammed Rashid
Keyword(s):  
Case Report ◽  
Infective Endocarditis ◽  
Rare Case ◽  
Case Reports ◽  
Multidrug Resistant ◽  
The Body ◽  
Prior History ◽  
Skin Reactions ◽  
Rare Case Report ◽  
Multiple Drugs

Rationale: Linezolid (LNZ) induced Cutaneous Adverse Drug Reactions (CADRs) have rare atypical presentation. Till date, there are very few published case reports on LNZ induced CADRs among the multidrug-resistant patients suffering from Infective Endocarditis (MDR IE). Here, we present a rare case report of LNZ induced CARs in a MDR IE patient. Case report: A 24-year-old female patient was admitted to the hospital with chief complaints of fever (101°C) associated with rigors, chills, and shortness of breath (grade IV) for the past 4 days. She was diagnosed with MDR IE, having a prior history of rheumatic heart disease. She was prescribed LNZ 600mg IV BD for MDR IE, against Staphylococcus coagulase-negative. The patient experienced flares of cutaneous reactions with multiple hyper-pigmented maculopapular lesions all over the body after one week of LNZ therapy. Upon causality assessment, she was found to be suffering from LNZ induced CADRs. LNZ dose was tapered gradually and discontinued. The patient was prescribed corticosteroids along with other supportive care. Her reactions completely subsided and infection got controlled following 1 month of therapy. Conclusion: Healthcare professionals should be vigilant for rare CADRs, while monitoring the patients on LNZ therapy especially in MDR patients as they are exposed to multiple drugs. Moreover, strengthened spontaneous reporting is required for better quantification.

scholarly journals Hyperhomocysteinemia in a Patient with Moyamoya Disease

2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
Durga Shankar Meena ◽  
Gopal Krishana Bohra ◽  
Mahadev Meena ◽  
Bharat Kumar Maheshwari
Keyword(s):  
Cerebrovascular Disease ◽  
Moyamoya Disease ◽  
Cerebral Angiography ◽  
Rare Case ◽  
Homocysteine Level ◽  
Case Reports ◽  
Circle Of Willis

Moyamoya disease is a chronic progressive cerebrovascular disease characterized by bilateral occlusion or stenosis of arteries around circle of Willis. We report a case of 18-year-old female presented with recurrent episodes of headache and vertigo. On cerebral angiography, the patient was diagnosed to have moyamoya disease. On further evaluation, thrombophilia profile showed increased homocysteine level. The patient was treated conservatively with cobalamin and aspirin and advised for revascularization. According to the literature, there are few case reports of moyamoya disease with thrombotic disorders. Hence, we are reporting this interesting and rare case.

Krukenberg tumor secondary to gall bladder carcinoma masquerading C3 glomerulopathy

2020 ◽  
Vol 4 (3) ◽  
pp. 105-108
Author(s):  
Priti Meena ◽  
Vinant Bhargava ◽  
Devinder Singh Rana ◽  
Anil Kumar Bhalla ◽  
Ashwani Gupta ◽  
...  
Keyword(s):  
Gall Bladder ◽  
Bladder Carcinoma ◽  
Case Reports ◽  
Abdominal Distension ◽  
Gastrointestinal Neoplasms ◽  
Solid Organ ◽  
Krukenberg Tumor ◽  
C3 Glomerulopathy ◽  
Gall Bladder Carcinoma ◽  
Loss Of Appetite

Background: C3 glomerulopathy is caused by dysregulation of the alternative complement pathway. Association with solid organ tumors is rare. However, there have been a few case reports of membranoproliferative glomerulonephritis secondary to gastrointestinal neoplasms. Case: A 38-year-old female presented with abdominal distension, loss of appetite, amenorrhea, and easy fatigability. She had been diagnosed 8 months back with C3 glomerulopathy and had received immunosuppression. On evaluation, she was incidentally detected to have Krukenberg tumor. The primary site of malignancy was gall bladder. Conclusion: Our case report highlights a possible association between C3 glomerulopathy and Krukenberg tumor secondary to gall bladder carcinoma and emphasizes the fact that even in cases of C3 glomerulopathy, occult malignancy should be considered as an underlying pathology.

scholarly journals Overt Skeletal Metastases in a Patient of Occult (Microscopic) Follicular Thyroid Carcinoma: a Rare Case

2017 ◽  
Vol 9 (1) ◽  
pp. 68-70
Author(s):  
Chandan Kumar Jha ◽  
Vinita Agrawal ◽  
Anjali Mishra ◽  
P. K. Pradhan
Keyword(s):  
Thyroid Carcinoma ◽  
Rare Case ◽  
Follicular Thyroid Carcinoma ◽  
Skeletal Metastases
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