scholarly journals Acantholytic dyskeratotic acanthoma: A rare clinicopathological entity – A case report and review of literature

2020 ◽  
Vol 2 ◽  
pp. 115-118
Author(s):  
Nandakumar Gopinathan Nair ◽  
B. M. Athira
Keyword(s):  
Case Report ◽  
Special Reference ◽  
Unknown Etiology ◽  
Review Of Literature ◽  
Benign Condition ◽  
The Past ◽  
Long Duration ◽  
Epidermal Proliferation

Acantholytic dyskeratotic acanthoma (ADA) is a rare benign condition characterized by circumscribed epidermal proliferation displaying both acantholysis and dyskeratosis. It is of unknown etiology and pathogenesis. We report a case of ADA of long duration in a 75-year-old female along with a review of literature with special reference to cases reported during the past 10 years.

scholarly journals An increasing trend of bilateral tubal ectopic gestation reported over the past two decades: a case report and review of literature

2018 ◽  
Vol 7 (6) ◽  
pp. 2518
Author(s):  
Mayuri Ahuja ◽  
Archana Mehta ◽  
Neerja Goel ◽  
Shehla Jamal
Keyword(s):  
Case Report ◽  
Acute Abdomen ◽  
Similar Case ◽  
Review Of Literature ◽  
Intraoperative Diagnosis ◽  
The Past ◽  
Ectopic Gestation ◽  
Increasing Trend ◽  
Ectopic Pregnancies

Bilateral tubal ectopic pregnancies which are spontaneously conceived are of rare occurrences. Generally, they are diagnosed intra-operatively. There are no guidelines published till date for their management. There has been a reported increase in the incidence of such cases. We present a review of such cases reported over the last two decades and report a similar case which presented to our hospital with acute abdomen and USG suggested hemo-peritoneum with further intraoperative diagnosis of bilateral tubal ectopic managed by left salpingectomy and right salpingostomy

scholarly journals Multicentric Cutaneous Crohn's Disease: A Case Report and Review of Literature

1990 ◽  
Vol 4 (2) ◽  
pp. 59-63 ◽  
Author(s):  
Robert Prokopetz ◽  
J Barrie Ross ◽  
Peter Smith ◽  
Joseph J Sidorov
Keyword(s):  
Crohn’S Disease ◽  
Case Report ◽  
Crohn's Disease ◽  
Erythema Nodosum ◽  
Skin Lesions ◽  
Review Of Literature ◽  
Histological Features ◽  
The Past ◽  
Common Skin ◽  
Skin Conditions

A patient presented with skin lesions at sites not contiguous with Crohn's disease of the bowel and with specific histological features of Crohn's disease occurring two weeks from the onset of bowel symptoms. Currently a number of nonspecific skin conditions such as erythema nodosum, pyoderma gangrenosum and erythema multiforme are accepted as being the most common skin manifestations of Crohn's disease. It is likely, however, that specific lesions of Crohn's disease in the skin have been underdiagnosed either because of lack of biopsy or misinterpretation of the histology. Twenty-three cases with specific Crohn's disease in the skin have been recorded in the past 25 years, since the condition has been recognized. Sarcoidosis has been a common misdiagnosis. The literature relating to multicentric Crohn's disease is reviewed and attention drawn to its protean and masquerading features. An argument is made for the use of the term 'multicentric' rather than 'metastatic' in relation to cutaneous Crohn's disease.

Reiter's Syndrome in Children: Case Report and Review of Literature

1962 ◽  
Vol 1 (3) ◽  
pp. 148-151
Author(s):  
Andrew M. Margileth
Keyword(s):  
Rheumatoid Arthritis ◽  
Case Report ◽  
Juvenile Rheumatoid Arthritis ◽  
No Value ◽  
Recent Literature ◽  
Classical Case ◽  
Review Of Literature ◽  
Reiter's Syndrome ◽  
The Past ◽  
Reiter’S Syndrome

1. Our experience with a six-year-old boy who had diarrhea, urethritis, conjunctivitis and arthritis is presented as a classical case of Reiter's syndrome. The patient recovered fully in a period of five months and has remained well during the past five years. 2. The cause of Reiter's syndrome remains unknown but in children may be related to Flexner bacillus dysentery. 3. The disease in children is usually less severe than in adults and all 11 children reported have recovered. The recent literature is reviewed. 4. Treatment with antibiotics is of no value and steroid therapy has not prevented exacerbations nor shortened the course of the disease. 5. The nongonococcal triad of urethritis, conjunctivitis, and arthritis is a distinct clinicopathologic entity which differs from known infections and juvenile rheumatoid arthritis.

scholarly journals Oral focal mucinosis of gingiva - a rare case report and review of literature

2017 ◽  
Vol 5 (1) ◽  
pp. 26
Author(s):  
Chandini Dabbiru ◽  
Raghavendra Mahadev Naik ◽  
Kishore Moturi ◽  
Govind Rajkumar
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Rare Case ◽  
Histopathological Examination ◽  
Excisional Biopsy ◽  
Unknown Etiology ◽  
Review Of Literature ◽  
Soft Tissue Lesion ◽  
Rare Case Report ◽  
Myxoid Degeneration

Oral focal mucinosis (OFM) is a rare soft-tissue lesion of unknown etiology. Clinically it appears as asymptomatic round lesions and histologically, characterized by focal myxoid degeneration of connective tissue with presence of stellate shaped fibroblasts which were also evident in the present case. This case report stresses on the fact that diagnosis of OFM is almost impossible hence diagnosis should be confirmed by histopathological examination following incisional or excisional biopsy. Through this article we present a rare case of one such lesion on the gingiva and enumerate the most characteristic and myxomatous lesions. Thus though rare, OFM must be considered in the differential diagnosis of soft tissue overgrowths in oral cavity. Here, we describe the clinical and histopathological   presentation and subsequent management of OFM in a female patient.

scholarly journals RENAL ONCOCYTOMA: A CASE REPORT WITH SPECIAL REFERENCE TO HISTOPATHOLOGY AND REVIEW OF LITERATURE

1983 ◽  
Vol 74 (3) ◽  
pp. 436-445 ◽  
Author(s):  
Shigeki Takahashi ◽  
Tsunetada Yazaki ◽  
Yoshihide Ogawa ◽  
Shori Kano ◽  
Ryuichi Kitagawa
Keyword(s):  
Case Report ◽  
Special Reference ◽  
Renal Oncocytoma ◽  
Review Of Literature

scholarly journals Total Hip Arthroplasty after McMurray’s Osteotomy – A Case Report and Review of Literature

2021 ◽  
Vol 11 (4) ◽  
Author(s):  
Sangeet Gawhale ◽  
Sagar Bansal ◽  
Amit Yadav ◽  
Shaswat Mishra ◽  
K S Akshay ◽  
...  
Keyword(s):  
Case Report ◽  
Total Hip Arthroplasty ◽  
Range Of Motion ◽  
Hip Arthroplasty ◽  
Review Of Literature ◽  
Total Hip ◽  
The Past ◽  
Femoral Stems ◽  
Operative Outcome ◽  
History Of

Introduction: Total hip arthroplasty after McMurray’s osteotomy increases the operative difficulties and decreases the chances of better outcome. With the advent of modular femoral stems, minute changes can be done to individual joints, which allow intraoperative flexibility and better post-operative outcome. Thus, it should be considered as an option for complicated cases. Case Report: We report a case of a 35-year-old female with chief complain of pain in the left hip while walking for the past 2 years. The patient also had difficulty in squatting and sitting cross legged. History of fracture in the left hip at 4 years of age for which McMurray’s osteotomy was done. The patient was operated with total hip arthroplasty using modular Sivash range of motion (S-ROM) stem. Conclusion: Modular S-ROM total hip arthroplasty is a good option for treatment in cases with previous osteotomy in femur. Keywords: McMurray’s osteotomy, total hip arthroplasty, Sivash range of motion.

scholarly journals Reticular Erythematous Mucinosis (REM): Case Report and Review of Literature

2018 ◽  
Author(s):  
Roxanne Rajaii ◽  
Summer Moon ◽  
Timothy Nyckowski ◽  
John Pui ◽  
Michael Mahon
Keyword(s):  
Case Report ◽  
Treatment Approach ◽  
Treatment Options ◽  
Sun Exposure ◽  
Pathological Diagnosis ◽  
Rare Disorder ◽  
Unknown Etiology ◽  
Review Of Literature ◽  
Classic Case

Reticular erythematous mucinosis (REM) is a rare disorder with an unknown etiology. REM requires both a clinical and a pathological diagnosis. Multiple relevant associations and triggers are known. Herein, we report a classic case of REM, whose condition was found to be correlated with smoking and exacerbated by sun exposure. Our diagnostic and treatment approach is based on a worldwide review of current research, and this report aims to demonstrate a classical presentation of REM and available treatment options that have proved efficacious to date.

scholarly journals Impaled Nasopharyngeal Foreign Body

2021 ◽  
Vol 28 (3) ◽  
pp. 285-288
Author(s):  
Pritam Chatterjee ◽  
V D Prasanna Kumar Vasamsetty ◽  
Chiranjib Das ◽  
Sudip Kumar Das
Keyword(s):  
Case Report ◽  
Foreign Body ◽  
Extensive Review ◽  
Review Of Literature ◽  
Vascular Surgeon ◽  
Unusual Site ◽  
Interventional Radiologist ◽  
Unusual Foreign Body ◽  
The Past ◽  
Impacted Foreign Body

Introduction Foreign body cases are common in otolaryngologic practice, usually occurring in children. An impacted penetrating impaling foreign body can be one of the most challenging emergencies Management revolves around safe extraction of impaling object and prevention of complications. Here we share our experience with one such case of unusual foreign body impacted at an unusual site, with an extensive review of  literature discussing management & prevention of complications in similar cases. Case Report A 3 year old boy presented to us in ENT emergency with a long metallic hook impaled in nasopharynx for the past 8 hours.  We were able to dislodge the impacted foreign body under direct endoscopic visualisation under general anaesthesia. Discussion Any such injury might be similar but no two injuries are the same. It needs combined expertise of multidisciplinary team usually consisting of  ENT surgeon, anaesthesiologist, radiologist and may also need vascular surgeon and interventional radiologist at times. Several complications are reported in literature, knowledge of which would help preparedness and thus a better outcome.

scholarly journals Kimura Disease: A case report and review of literature

2018 ◽  
Vol 17 (1) ◽  
pp. 152-154
Author(s):  
Partha Pratim Sinha Roy ◽  
Parthasarathi Ghosh ◽  
Dwaipayan Samaddar ◽  
Gautam Das
Keyword(s):  
Case Report ◽  
Inflammatory Disease ◽  
Medical Science ◽  
Neck Region ◽  
Chronic Inflammatory Disease ◽  
Unknown Etiology ◽  
Review Of Literature ◽  
Kimura Disease ◽  
Head And Neck Region ◽  
Blood Eosinophilia

Kimura disease is a rare chronic inflammatory disease with angiolymphatic proliferation of unknown etiology predominantly seen among young Asian males. It classically shows a triad of non-tender subcutaneous masses predominantly in head and neck region with tissue and blood eosinophilia and raised serum IgE level. Here we present a case report of a 24 years male with bilateral pre-auricular and post-auricular swelling for 6 years. The diagnosis of Kimura disease was made on the basis of clinical and histopathological examination.Bangladesh Journal of Medical Science Vol.17(1) 2018 p.152-154

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