scholarly journals Syphilitic Balanitis of Follmann, A Rare Case Report

2021 ◽  
Vol 19 (1) ◽  
pp. 71-73
Author(s):  
Pooja Agarwal ◽  
Ashish Jagati ◽  
Priyanka Vadher ◽  
Malay Chaudhary
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Presentation ◽  
Heterosexual Male ◽  
Primary Syphilis ◽  
Rare Case Report

Syphilitic balanitis of Follmann is a rare presentation of primary syphilis. It can occur before or after the appearance of primary chancre and some time without any associated primary chancre. We are reporting a case of syphilitic balanitis of Follmann, in a 23 years old heterosexual male, who presented with balanitis associated with single indurated lesion over coronal sulcus and few superficial ulcers over prepuce.

scholarly journals Psoriasiform Mycosis Fungoides Involving the Face- A Rare Case Report

2021 ◽  
pp. 94-99
Author(s):  
N. R. Vignesh ◽  
Shreya Srinivasan ◽  
G. Sukanya ◽  
S. Arun Karthikeyan
Keyword(s):  
Case Report ◽  
Mycosis Fungoides ◽  
Rare Case ◽  
Cell Lymphoma ◽  
Punch Biopsy ◽  
Cutaneous T Cell Lymphoma ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Atypical Cells ◽  
The Face

Mycosis fungoides is represented as the most common epidermotropic cutaneous T-cell lymphoma, which is mainly characterized by the proliferation of atypical cells within the epidermis. We report a rare presentation of mycosis fungoides in a 60-year-old male presenting with chronic psoriasiform plaque involving the face. Punch biopsy of the lesion from the forehead was taken for routine histological examination and immunohistochemical stains. Results of biopsy and immunohistochemical findings were consistent with mycosis fungoides and diagnosed as psoriasiform presentation of mycosis fungoides involving the face.

scholarly journals Hypercalcemia in a patient with SLE and antiphospholipid antibody syndrome: a rare case report from Bangladesh

2014 ◽  
Vol 2 (1) ◽  
pp. 35-37
Author(s):  
G Dewan
Keyword(s):  
Case Report ◽  
Primary Hyperparathyroidism ◽  
Rare Case ◽  
Adult Patients ◽  
Antiphospholipid Antibody ◽  
Antiphospholipid Antibody Syndrome ◽  
Medical Sciences ◽  
Rare Presentation ◽  
Initial Report ◽  
Rare Case Report

Association of hypercalcemia with SLE is very rare. Since initial report in 1991 only hand full cases have been described mainly in adult patients sporadically. Three pattern observed in this rare presentation. Commonly it is associated with serositis and lymphadenopathy or lymphedema known as hypercalcemia-lymphadenopathy SLE {HL-SLE) or hypercalcemia- lymphedema syndrome. Second group do not show this particular association. Concomitant primary hyperparathyroidism is responsible for third variety. This report describes a case of hypercalcemia associated with SLE from Bangladesh. DOI: http://dx.doi.org/10.3126/jucms.v2i1.10490   Journal of Universal College of Medical Sciences (2014) Vol.2(1): 35-37

scholarly journals A Rare Case Report- An Incidental Finding of Isolated Unilocular Splenic Hydatid Cyst

2021 ◽  
pp. 259-265
Author(s):  
Shubham Satyaprakash Gupta ◽  
Sangita Jogdand Shinde ◽  
Raju K. Shinde ◽  
Shweta Pandey
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Rare Case ◽  
Unusual Case ◽  
Incidental Finding ◽  
Abnormal Uterine Bleeding ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Total Splenectomy ◽  
Splenic Hydatid Cyst

Splenic Hydatid Cyst is a very rare presentation with less than 5% of total incidences of Cystic Echinococcosis. It is usually due to spread of cysts from other regions leading to secondaries. Primary isolated splenic hydatid cyst without involvement of any other organs is even rarer. We report an unusual case of a female who presented as Abnormal Uterine Bleeding (AUB) with an incidental finding of Isolated Splenic Hydatid Cyst with absence of involvement of any other organ. Patient underwent laparotomy and total splenectomy was done. This case report targets to report a rare case of incidental finding of isolated unilocular hydatid cyst of spleen and describes its management.

scholarly journals Neonatal Umbilical Myiasis- A Rare Case Report

2021 ◽  
Author(s):  
Sonu Kumar ◽  
Poonam Dalal ◽  
. Neha ◽  
Ankit Singla
Keyword(s):  
Emergency Department ◽  
Case Report ◽  
Vaginal Delivery ◽  
Rare Case ◽  
Index Case ◽  
Normal Vaginal Delivery ◽  
Wild Animals ◽  
Rare Presentation ◽  
Rare Case Report ◽  
Male Neonate

Myiasis is an infestation of live vertebrates (humans and/or animals) by larvae of dipterous fly. Although, it usually infects domestic and wild animals but humans may be rarely affected if they are reared in unhygienic condition. The index case is a seven-day-old male neonate born by normal vaginal delivery, who presented to the Emergency Department with complaint of passage of worms from umbilicus which do not extend to deeper tissues. On examination, periumbilical erythema was also visible along with white glistening worms. After application of turpentine oil to the umbilical stump, the worms were mechanically removed with the help of forceps. Umbilical myiasis is a very rare presentation indicating poor hygiene and a preventable condition.

scholarly journals Primary tubercular otitis media: a rare case report

2019 ◽  
Vol 5 (6) ◽  
pp. 1723
Author(s):  
Vishal Sharma ◽  
Sanjeev Bhagat ◽  
Dimple Sahni ◽  
Dinesh Sharma
Keyword(s):  
Case Report ◽  
Otitis Media ◽  
Rare Case ◽  
Fine Needle Aspirate ◽  
Rare Presentation ◽  
Fine Needle ◽  
Acid Fast Bacilli ◽  
Rare Case Report ◽  
Tuberculosis Diagnosis ◽  
High Index Of Suspicion

<p class="abstract">Tubercular otitis media is a rare presentation of tuberculosis. High index of suspicion is required for diagnosis. We present a rare case of tubercular otitis media presenting as post auricular swelling with no evidence of pulmonary or any other foci of tuberculosis. Diagnosis was made on the basis of acid fast bacilli seen in fine needle aspirate. Anti-tubercular drugs were initiated and patient responded well to treatment.</p><p class="abstract"> </p>

scholarly journals Preauricular Sinus as Recurrent Postaural Abscess: A Rare Presentation

2014 ◽  
Vol 6 (2) ◽  
pp. 84-86 ◽  
Author(s):  
Sharanabasappa Rudragouda Malipatil
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Rare Case ◽  
Sinus Tract ◽  
Recurrent Infections ◽  
Rare Presentation ◽  
Treatment Patient ◽  
Preauricular Sinus ◽  
Rare Case Report ◽  
Surgical Extirpation

ABSTRACT Preauricular sinus (PAS) is not uncommon congenital anomaly. It is usually asymptomatic and does not require any treatment. Patient presenting with discharge, recurrent infections and preauricular abscess will require management with antibiotics and surgical extirpation of the sinus tract. Here, it is a rare case report of PAS presenting as a recurrent postaural abscess. How to cite this article Malipatil SR. Preauricular Sinus as Recurrent Postaural Abscess: A Rare Presentation. Int J Otorhinolaryngol Clin 2014;6(2):84-86.

scholarly journals Preauricular Sinus as Recurrent Postaural Abscess: A Rare Presentation

2015 ◽  
Vol 7 (1) ◽  
pp. 26-28
Author(s):  
Sharanabasappa Rudragouda Malipatil
Keyword(s):  
Congenital Anomaly ◽  
Case Report ◽  
Rare Case ◽  
Sinus Tract ◽  
Recurrent Infections ◽  
Rare Presentation ◽  
Treatment Patient ◽  
Preauricular Sinus ◽  
Rare Case Report ◽  
Surgical Extirpation

ABSTRACT Preauricular sinus (PAS) is not uncommon congenital anomaly. It is usually asymptomatic and does not require any treatment. Patient presenting with discharge, recurrent infections and preauricular abscess will require management with antibiotics and surgical extirpation of the sinus tract. Here, it is a rare case report of PAS presenting as a recurrent postaural abscess.

scholarly journals Complicated pseudodiverticulosis of small intestine: a rare case report

2019 ◽  
Vol 6 (9) ◽  
pp. 3433
Author(s):  
Kamal Raj M. ◽  
V. Venkatachalam ◽  
Manasa A.
Keyword(s):  
Small Intestine ◽  
Case Report ◽  
Diverticular Disease ◽  
Acute Abdomen ◽  
Large Bowel ◽  
Rare Case ◽  
Megaloblastic Anemia ◽  
Rare Presentation ◽  
Rare Case Report

Diverticular disease though being a common entity in large bowel is recently noted to occur more proximally as well. In the jejunum, the mucosal outpouchings, called as pseudo-diverticulae, occurs with an incidence of 0.5-1.5%.Diagnosed incidentally as majority of them remain asymptomatic. When they are symptomatic, dyspepsia and bloating, recurrent abdominal cramping, malabsorption and megaloblastic anemia occurs. On occasions it is not uncommon for patients to present with hemorrhage, infections, obstruction or perforation. Perforation, being a rare presentation occurs in less than 6% of the cases. We present a case of a 70 year old male, who presented as acute abdomen, found to have isolated jejunal diverticular perforation intraoperatively.

scholarly journals Appendicitis in epigastric hernia: a rare case report

2018 ◽  
Vol 5 (3) ◽  
pp. 1117
Author(s):  
Bárbara Da Silva Oliveira Fonseca ◽  
Luís Gustavo Origa ◽  
José Reinaldo Ribeiro De Queiroz Junior ◽  
Lucas Azevedo Faria ◽  
Fábio Pimentel Martins ◽  
...  
Keyword(s):  
Case Report ◽  
Acute Appendicitis ◽  
Rare Case ◽  
Anatomical Variation ◽  
Xiphoid Process ◽  
Epigastric Hernia ◽  
Rare Presentation ◽  
Pathophysiological Process ◽  
Rare Case Report ◽  
Belo Horizonte

Epigastric hernias are defined as defects in the abdominal midline between the navel and the xiphoid process. Incarceration and strangulation are rare. This is a case report, the purpose of this article is to report a case of acute appendicitis successfully treated in an incarcerated epigastric hernia at the Santa Casa de Misericórdia Hospital in Belo Horizonte, correlating with the current literature. It is not yet clear how the cecum and appendix can mobilize freely to the epigastric region and present within the sac of an epigastric hernia. It has been suggested that in 10% of the population, there may be anatomical variation and abnormal mobility of the cecum, referred to as mobile cecal syndrome. However, it is difficult to establish which pathophysiological process (or perhaps both) could have attributed to this rare presentation.

scholarly journals Recto-sigmoid neurofibroma presenting as rectal prolapse in an adult patient with neurofibromatosis - a rare presentation

2014 ◽  
Vol 13 (3) ◽  
pp. 356-357
Author(s):  
Shah Naveed ◽  
Hasina Quari ◽  
ShahNawaz Bashir ◽  
RK Chrungoo ◽  
Tanveer H Banday
Keyword(s):  
Case Report ◽  
Rectal Prolapse ◽  
Adult Patient ◽  
Rare Case ◽  
Medical Science ◽  
Rare Presentation ◽  
Rare Case Report

Neurofibroma occurs most frequently in the stomach and jejunum, but the colon may also be involved. Its association with rectal prolapse has not been reported yet. We are reporting here such a rare case report. DOI: http://dx.doi.org/10.3329/bjms.v13i3.15657 Bangladesh Journal of Medical Science Vol.13(3) 2014 p.356-357

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