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

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 OF PARATESTICULAR RHABDOMYOSARCOMA IN AN ADULT PATIENT

2021 ◽  
Vol 71 (2) ◽  
pp. 724-26
Author(s):  
Mussadique Ali ◽  
Chandumal . ◽  
Manzoor Khan ◽  
Jhanzeb Iftikhar ◽  
Samia Yasmeen ◽  
...  
Keyword(s):  
Case Report ◽  
Complete Remission ◽  
Adult Patient ◽  
Rare Case ◽  
Embryonal Rhabdomyosarcoma ◽  
Childhood And Adolescence ◽  
Solid Mass ◽  
Mesenchymal Tissue ◽  
Rare Case Report ◽  
Tissue Origin

Rhabdomyosarcoma is a malignancy of mesenchymal tissue origin typically occurring in childhood and adolescence, with an incidence rate of of 4.3 patients per million population per anum. Primary rhabdomyosarcoma of para-testicular origin is an infrequent condition, making up to 7% of all the cases of rhabdomyosarcoma tumors in children and adolescents. Here we describe a case of a 25 years old man with left paratesticular solid mass. He underwent left sided orchiectomy with histopathology revealing paratesticuler embryonal rhabdomyosarcoma. He underwent definitive chemo-radiotherapy and orchidopexy with complete remission and is on active surveillance for 4 years.

scholarly journals Primary intracranial peripheral primitive neuroectodermal tumor in an adult patient with aphasia: a rare case report

2021 ◽  
Author(s):  
kazem ghaemi ◽  
mahdieh rajabi-moghaddam ◽  
Hamid Abbaszadeh
Keyword(s):  
Case Report ◽  
Adult Patient ◽  
Rare Case ◽  
Primitive Neuroectodermal Tumor ◽  
Chief Complaint ◽  
Peripheral Primitive Neuroectodermal Tumor ◽  
Primitive Neuroectodermal Tumors ◽  
Neuroectodermal Tumors ◽  
Rare Case Report ◽  
First Time

Primary intracranial primitive neuroectodermal tumors (PNETs) are extremely rare malignancies, affects children and adolescents with only 10 cases has been reported over 33 years old. we present a case of PNET in a 36 years old female patient with the chief complaint of aphasia for the first time

scholarly journals A Rare Case Report: Bilateral Choanal Atresia in an Adult Patient

2020 ◽  
Vol 3 (1) ◽  
pp. 26-28
Author(s):  
Ayhan Kars ◽  
◽  
Fatih Bingol ◽  
Fatma Atalay ◽  
◽  
...  
Keyword(s):  
Case Report ◽  
Adult Patient ◽  
Rare Case ◽  
Choanal Atresia ◽  
Rare Case Report

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.

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