scholarly journals Steatocystoma Multiplex of Scortum- Rare Genetic Disorder: A Case Report and Review of Literature

2016 ◽  
Vol 33 (4) ◽  
pp. 218-221
Author(s):  
Moni Mohan Saha ◽  
Sukumar Saha ◽  
Ratan Lal Datta Banik ◽  
Md Mokter Hossain
Keyword(s):  
Case Report ◽  
Microscopic Examination ◽  
Autosomal Dominant ◽  
Genetic Disorder ◽  
Review Of Literature ◽  
Dominant Mutation ◽  
College Hospital ◽  
Medical College ◽  
Steatocystoma Multiplex ◽  
Keratin 17

A 25 years old male attended the skin & VD outpatient department of Khulna Medical College Hospital on 16th June, 2013 with complaints of multiple asymptomatic small rounded firm, cystic nodules that are adherent to the overlying skin of scortum. The microscopic examination of the cystic nodules showed the features of steatocystoma multiplex. This disorder, although it is asymptomatic, is a cosmetic threat to the patient. Only a few cases of the patients with an autosomal dominant mutation, who had keratin 17; have been reported. We are reporting here a case of steatocystoma multiplex of scortum in a 25 years old male along with review of literature.J Bangladesh Coll Phys Surg 2015; 33(4): 218-221

scholarly journals Chorangioma - A Case Report

2014 ◽  
Vol 14 (2) ◽  
pp. 185-186
Author(s):  
Rehana Khanam ◽  
P.K. Ghosh ◽  
Fauzia Jahan ◽  
Saidur Rahman
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Live Birth ◽  
Microscopic Examination ◽  
Histopathological Examination ◽  
Incidental Finding ◽  
Caesarian Section ◽  
College Hospital ◽  
Medical College ◽  
Clinically Normal

We present a female patient with pregnancy associated with normal live birth and the unusual concomitance of chorangioma. It was an incidental finding during the routine microscopic examination of the placenta of the 30 year multipara whose pregnancy was clinically normal. She was admitted to the Bangladesh Medical College Hospital for labor at 34 weeks gestation. She was investigated thoroughly because of irregular pervaginal bleeding before delivary. Caesarian section was done at 37th weeks of pregnancy. The placenta was found enlarged, irregular and haemorrhagic. Histopathological examination from the sections of specimen was done and diagnosed as Chorangioma. The case is presented as below.DOI: http://dx.doi.org/10.3329/jom.v14i2.19671 J Medicine 2013, 14(2): 185-186

scholarly journals Unusual presentation of a Hydatid cyst: a case report

2015 ◽  
Vol 22 (2) ◽  
pp. 216-218 ◽  
Author(s):  
Asifa Sattar ◽  
Nazmun Nahar ◽  
Md Mizanur Rahman ◽  
ASM Tanim Anwar ◽  
Anwar Hossain
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Echinococcus Granulosus ◽  
Hydatid Disease ◽  
The Body ◽  
Unusual Presentation ◽  
Parasitic Disease ◽  
College Hospital ◽  
Medical College ◽  
The World

Hydatid disease is a parasitic disease, which is most commonly caused by Echinococcus granulosus. It is endemic in many parts of the world. However, Hydatid disease can occur in almost any part of the body. Isolated omenal hydatid cyst is one of the least common sites. A case of very unusual omental hydatid cyst is presented here which was diagnosed in the Department of Radiology & Imaging, Dhaka Medical College Hospital, Dhaka, and subsequently confirmed by histopathology. DOI: http://dx.doi.org/10.3329/jdmc.v22i2.21546 J Dhaka Medical College, Vol. 22, No.2, October, 2013, Page 216-218

scholarly journals Diagnosis of Achondroplasia at Birth: A Case Report

2020 ◽  
Vol 58 (222) ◽  
Author(s):  
Suzit Bhusal ◽  
Uttara Gautam ◽  
Rajan Phuyal ◽  
Robin Choudhary ◽  
Sunil Raja Manandhar ◽  
...  
Keyword(s):  
Case Report ◽  
Vaginal Delivery ◽  
Autosomal Dominant ◽  
Fibroblast Growth Factor Receptor ◽  
Genetic Disorder ◽  
Radiological Finding ◽  
Growth Factor Receptor ◽  
Fibroblast Growth ◽  
Spontaneous Vaginal Delivery ◽  
Antenatal Ultrasonography

Autosomal dominant mutations in fibroblast growth factor receptor 3 cause achondroplasia, the most common form of dwarfism in humans. Achondroplasia is a genetic disorder causing rhizomelic shortening of limbs. Head is often large with prominent forehead causing vaginal delivery difficult. A twenty-one years old multipara mother gave birth to a baby with achondroplasia via spontaneous vaginal delivery with episiotomy without any complication. Achondroplasia, in this case, was diagnosed on the basis of antenatal ultrasonography finding, clinical features and radiological finding of the baby. He was admitted in the special baby care unit for observation and discharged on the next day as no complications were noted.

scholarly journals Gorlin-Goltz Syndrome - An Unusual Case Report

2016 ◽  
Vol 5 (1) ◽  
pp. 1071
Author(s):  
B. Thayumanavan ◽  
T. Jeyanthikumari ◽  
P. Meghalapriya
Keyword(s):  
Case Report ◽  
Unusual Case ◽  
Autosomal Dominant ◽  
Keratocystic Odontogenic Tumor ◽  
Review Of Literature ◽  
Autosomal Dominant Disorder ◽  
Goltz Syndrome ◽  
Multisystemic Disease ◽  
Consistent Feature ◽  
Unusual Case Report

Gorlin-Goltz syndrome is an uncommon autosomal dominant disorder manifesting as a multisystemic disease. Keratocystic odontogenic tumor (KCOT) is considered as the most consistent feature of this syndrome. Dentists play a key role in making early diagnosis of this syndrome. Here we present a case of Gorlin- Goltz syndrome identified by multiple multilocular radiolucencies in the mandible. A review of literature of different diagnostic criteria for Gorlin-Goltz syndrome is also discussed.

scholarly journals Hepatic Lobectomy-Case Report of Two Patients, Performed at Chittagong Medical College Hospital

1970 ◽  
Vol 26 (3) ◽  
pp. 153-157
Author(s):  
SM Ashraf Ali ◽  
Md Margub Hussain
Keyword(s):  
Case Report ◽  
Life Experience ◽  
Left Lobe ◽  
Medical College Hospital ◽  
General Surgeon ◽  
College Hospital ◽  
Socioeconomic Condition ◽  
Low Socioeconomic ◽  
Medical College ◽  
Tertiary Center

Lobectomy of liver is indicated for different conditions; mainly malignancy and trauma. Though it is highly specialized operation and preferably be performed in specialized tertiary center, sometime a general surgeon may not be in a position to avoid the surgery due to very low socioeconomic condition or to tackle emergency traumatic condition. Two case report of Lobectomy of liver; right lobectomy for hepatocellular carcinoma, and left lobectomy for left lobe big cyst and multiple stones in it were performed at Chittagong Medical College Hospital utilizing the existing facilities. Both patients recovered uneventfully. Case I expired after two month and fourteen day, Case II leading a pain free cheerful normal life. Experience of management of these two cases of resection of liver is recorded at Chittagong Medical College Hospital. DOI: 10.3329/jbcps.v26i3.4201 J Bangladesh Coll Phys Surg 2008; 26: 153-157

scholarly journals Fordyce's Disease Treated with Pimacrolimus: A Rare Case Report

2018 ◽  
Vol 9 (2) ◽  
pp. 148-151
Author(s):  
Tania Hoque ◽  
AZM Maidul Islam
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Medical College Hospital ◽  
Rare Disorder ◽  
College Hospital ◽  
Medical College ◽  
Rare Case Report ◽  
Lip Biopsy

Fordyce's disease, a rarely found disease of lips has been reported recently in department of Skin and VD, Gonosashthaya Somaj Vittic Medical College Hospital, Savar, Dhaka. Occasionally it may not be possible to identify the cause. The patient presented with identical features of Fordyce's disease and lip biopsy for histopathology showed the features of Fordyce's disease. Then patient was treated with Pimecrolimus cream and improved. Fordyce's disease is an extremely rare disorder. So its cutaneous findings, histopathology and treatments are highlighted here.Anwer Khan Modern Medical College Journal Vol. 9, No. 2: Jul 2018, P 148-151

scholarly journals Do you know this syndrome?

2013 ◽  
Vol 88 (3) ◽  
pp. 473-475 ◽  
Author(s):  
Laura Maria Andrade Silveira ◽  
Andreia Nogueira Ramos ◽  
Isadora Rosado do Amaral ◽  
Vitoria Regina Pedreira de Almeida Rego
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Autosomal Dominant ◽  
Congenital Abnormalities ◽  
Clinical Presentation ◽  
Current Knowledge ◽  
Genetic Disorder ◽  
Mucous Membranes ◽  
Form Part

Congenital Hypertrichosis Lanugionsa is a rare autosomal dominant genetic disorder, with fewer than 50 cases reported in the literature. It is characterized by excessive lanugo hair, sparing only the mucous membranes, palms and soles. It may be associated with other organic abnormalities and should form part of the dermatologist's current knowledge. We discuss some aspects of the syndrome in question arising from the case report of a 2-year-old female patient, black, with classic clinical presentation, with no other associated congenital abnormalities.

scholarly journals Jejunogastric Intussusception: A Case Report

2012 ◽  
Vol 30 (1) ◽  
pp. 44-47 ◽  
Author(s):  
MM Hussain ◽  
A Rahman ◽  
MR Abedin ◽  
MA Habib
Keyword(s):  
Emergency Department ◽  
Abdominal Pain ◽  
Case Report ◽  
Early Diagnosis ◽  
Medical College Hospital ◽  
College Hospital ◽  
Medical College ◽  
Prompt Treatment ◽  
Jejunogastric Intussusception ◽  
Acute Form

Jejunogastric intussusception is an established complication following any type of gastroenterostomy. In its acute form it presents with abdominal pain and lump suggestive of obstruction. It is also a rare cause of haematemesis. Chronic and intermittent presentation has also been described. It is a surgical emergency in its acute form. Early diagnosis and prompt treatment is required to avoid mortality. We report here a case that had a history suggestive of recurrent symptoms and ultimately presented as an acute emergency in the emergency department of Dhaka Medical College Hospital, Dhaka, Bangladesh   DOI: http://dx.doi.org/10.3329/jbcps.v30i1.11366   J Bangladesh Coll Phys Surg 2012; 30: 44-47  

scholarly journals Porokeratosis mibelli- A Case Report

1970 ◽  
Vol 17 (2) ◽  
pp. 106-107
Author(s):  
MA Siddiqui ◽  
MR Kabir ◽  
SM Badruddoza ◽  
AA Amin
Keyword(s):  
Case Report ◽  
Ankle Joint ◽  
Left Thigh ◽  
Small Satellite ◽  
Medial Aspect ◽  
College Hospital ◽  
Linear Fashion ◽  
Medical College ◽  
Upward Direction ◽  
The Individual

A twelve years old girl of class VII reported at skin & VD out patient department of Rajshahi Medical college Hospital in November 2003 with multiple small pink to violeceous non pruritic patches extending from medial aspect of left ankle joint to the medial aspect of left thigh in a linear fashion. The individual lesions are small-circumscribed patches having hyperkeratotic margin and central atrophy. The raised hyperkeratotic margin contains on its top a furrow along the course of the wall. The surface was verrucous and many of the lesions have serpiginous border. Near the ankle joint and below the ankle joint individual lesion forms zosteriform groups. On the thigh the lesions are linear. Some small satellite lesions are also present. All the lesions are hairless and anhidrotic. The onset of the individual lesions was at the age of six years, near the ankle joint. Lesions enlarge slowly and progressed to upward direction in a linear fashion. Skin biopsy for histopathology revealed the picture of porokeratosis. doi: 10.3329/taj.v17i2.3457 TAJ 2004; 17(2):  106-107

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