scholarly journals When the story doesn’t fit

2016 ◽  
Vol 85 (2) ◽  
pp. 74-76
Author(s):  
Jason L Elzinga ◽  
Charles Jian

Melanoma is an aggressive but easily preventable cancer. However, it may have a highly atypical presentation which makes early detection more difficult. This case report discusses a 25-year-old patient with a rare case of melanoma developing underneath the nail of the first toe. The case was originally diagnosed as trauma due to its rarity and epidemiological unlikeliness, however through the patient’s persistence for alternative opinions the correct diagnosis was eventually made. However, this led to an amputation as well as more intense, invasive treatment. There were several points on history (duration of the lesion, appearance of the lesion, and lack of healing progress) which when combined with the lesion’s physical appearance should have made such a presentation suspicious for a more malignant cause. This case highlights the importance of early detection in the prognosis and treatment of patients with cancer, the importance of considering all aspects of a history and physical exam, and the importance of listening to and addressing a patient’s concerns. As always, more common diagnoses should be first considered, but when the story does not match up with the presentation, one should move past the horses to consider the zebras.

Medicina ◽  
2022 ◽  
Vol 58 (1) ◽  
pp. 132
Author(s):  
Hsiao-Yun Chao ◽  
Chih-Huang Li ◽  
Shou-Yen Chen

Endoscopic biliary stent insertion is a well-established procedure that is indispensable in the management of various benign and malignant biliary disorders, and one that helps prevent mortality related to invasive surgical procedures. We report a rare case of the distal migration of a biliary stent outside the abdomen to the pericardium, inducing constrictive pericarditis and septic shock. This case alerts clinicians to be aware of potential adverse events that can lead to unfavorable patient outcomes. Such adverse events can be effectively avoided through early detection and intervention.


Cureus ◽  
2021 ◽  
Author(s):  
Raed Atiyat ◽  
Sindhusha Veeraballi ◽  
Neveen Al-Atiyat ◽  
Kok Hoe Chan ◽  
Jihad Slim

2021 ◽  
pp. 20210033
Author(s):  
Poonamjeet Loyal ◽  
Samuel Gitau ◽  
Soraiya Manji ◽  
Sitna Mwanzi ◽  
John Weru

Hepatocellular carcinoma (HCC) is the most common primary cancer of the liver and a major cause of mortality globally. Atypical presentation of HCC can present a diagnostic challenge. We, therefore, present a rare case of hepatocellular carcinoma fungating through the anterior abdominal wall with concomitant lung and brain metastases in a young patient with non-cirrhotic liver but positive chronic hepatitis B serology.


2021 ◽  
Vol 3 (1) ◽  
pp. 36-39
Author(s):  
Arunima ◽  
Vipin Ahuja

Eruption of tooth at about 6 months of age is a momentous stage in child’s life and is an emotional event for the parents. Though, a tooth present in the oral cavity of new born can lead to a lot of delusions. The occurrence of natal and neonatal teeth is a scarce anomaly, which for centuries has been associated with assorted superstitions among different ethnic groups. Natal teeth are more frequent than neonatal teeth, with the ratio being approximately 3: 1. Natal and neonatal teeth are of paramount importance not only for a dentist but also for a paediatrician since their presence may lead to numerous complications. Early detection and treatment of these teeth are recommended because they may induce deformity or mutilation of tongue, dehydration, inadequate nutrients intake by the infant, and growth retardation, the pattern and time of eruption of teeth and its morphology. This paper reports a rare case, wherein a neonatal tooth has led to the development of a fibrous hyperplasia in 10 months old infant.


2021 ◽  
Vol 7 (1) ◽  
pp. 87-89
Author(s):  
Rifat Taher Anne ◽  
Md Zakirul Islam ◽  
Farhana Noman ◽  
Ferdousi Hasnat ◽  
Shamima Sharmin Shova ◽  
...  

Although Coronavirus disease (COVID-19) can affect all age groups, severity of clinical presentation among children and newborns are milder than in adults. Along with classical symptoms, atypical presentation could be noted in the neonate. We report here a case of neonatal COVID-19 where a newborn infant presented with fever, lethargy, respiratory distress and recurrent seizure. Early detection and prompt management is the prerequisite for limiting transmission and reducing neonatal death rate. Journal of National Institute of Neurosciences Bangladesh, January 2021, Vol. 7, No. 1, pp. 87-89


2020 ◽  
Vol 10 (1) ◽  
Author(s):  
Taddei Edoardo ◽  
Sartori Elena ◽  
Raio Bulgheroni Luigi ◽  
Papadia Andrea

AbstractObjectivesEmanuel syndrome is a rare inherited syndrome, a correct in utero diagnosis allows effective management for ongoing and future pregnancies.Case presentationHere, we report a case of a complete non-mosaic trisomy 22, with several prenatal sonographic findings, that was diagnosed in utero at 15 weeks’ gestation and then it was confirmed with chromosomal analysis and postmortem examination.ConclusionsEvery anatomical difference should always be further investigated in order to achieve the correct diagnosis.


2019 ◽  
Vol 12 ◽  
pp. 117954761982868 ◽  
Author(s):  
Muhammad Ishaq Ghauri ◽  
Syeda Beenish Bareeqa ◽  
Amir Riaz ◽  
Ajeet Kumar

Introduction: Iatrogenic or physician-induced hypervitaminosis D is a rare cause of persistent vomiting. To the best of our knowledge, this is the first case report on iatrogenic hypervitaminosis D presenting with persistent vomiting in Pakistan. Case Report: We report a rare case of continual vomiting for 15 days in a 48-year-old woman of Pakistani descent. She was a known case of diabetes mellitus for 8 years, which was well controlled at the time of presentation. Conclusions: The correct diagnosis of our patient was based on clinical suspicion, appropriate lab tests, and deliberation of the differential diagnosis. It is important to consider hypervitaminosis D as a cause of persistent vomiting if no other obvious is apparent.


2012 ◽  
Vol 2012 ◽  
pp. 1-3
Author(s):  
Anshita Agarwal ◽  
Gaurav P. Agrawal ◽  
Sarwar Alam ◽  
Benazeer Husain

Eosinophilic granuloma of bone is a disease with an incidence of one new case per 350,000 to 2 million per year, which is an uncommon disease of maxillofacial region, and presents in more than 90% in children under the age of ten with predominance for males. As a result, eosinophilic granuloma of the jaw is always unconsidered in the differential diagnosis of similar lesions by many clinicians. It is difficult to make a correct diagnosis on it without proof of a pathological diagnosis, which correlates with the diverse clinical and radiographic presentations of eosinophilic granuloma in the jaws. In the present paper we report a rare case of unifocal eosinophilic granuloma of mandible occurring in an adult female.


2011 ◽  
Vol 3 (3) ◽  
pp. 227-232 ◽  
Author(s):  
Mohankumar Kurukumbi ◽  
Amruta Muley ◽  
Ganga Ramidi ◽  
Zakiya Wynn ◽  
Annapurni Jayam Trouth

Author(s):  
Daksh Gadi ◽  
Saket Nigam ◽  
Deepti Gupta ◽  
Akanksha Sinha

Tuberculosis is a major health problem in India and in view of rise in the MDR tuberculosis atypical presentations are getting commoner these days and are difficult to diagnose. Musculoskeletal tuberculosis is very common among the  hematogenous spread cases of pulmonary tuberculosis involving thoracic spine the most. Involvement of sacrum and coccyx is rarest of  the possibility and isolated sacrococcygeal tuberculosis thus is very rare. Being a rare entity a high index of clinical suspicion is required to diagnose it. We hereby report a very rare case report of sacrococcygeal tuberculosis.


Sign in / Sign up

Export Citation Format

Share Document