scholarly journals Intraorbital Cavernous Haemangioma (CHM)

1970 ◽  
Vol 6 (1) ◽  
pp. 32-33
Author(s):  
MS Rahman ◽  
MA Hossain
Keyword(s):  
Case Report ◽  
Optic Nerve ◽  
Ct Scan ◽  
Key Words ◽  
Rare Case ◽  
Armed Forces ◽  
Cavernous Haemangioma ◽  
Medical College ◽  
Computed Tomographic ◽  
Rare Case Report

This is an interesting and rare case report of right intraorbital cavernous haemangioma near optic nerve of a12 years boy who was hospitalized for right sided uniocular moderate axial proptosis and headache withoutany impairment of vision. Computed Tomographic (CT) scan showed fusiform enlargement of around rightoptic nerve just behind the eye ball. The mass was removed by right fronto-orbito-zygomatotomy incision anddiagnosed post-operatively as intraorbital cavernous haemangioma (CHM).Key words: Intraorbital cavernous haemangioma.DOI: 10.3329/jafmc.v6i1.5990Journal of Armed Forces Medical College, Bangladesh Vol.6(1) 2010 p.32-33

scholarly journals Unilateral lung hypoplasia presenting in seventh decade of life: a rare case report

2018 ◽  
Vol 5 (6) ◽  
pp. 1532
Author(s):  
Baishakhi Chandra ◽  
Bhaskar K. ◽  
Paramjyothi G. K.
Keyword(s):  
Case Report ◽  
Ct Scan ◽  
Lung Volume ◽  
Clinical Condition ◽  
Rare Case ◽  
Pulmonary Hypoplasia ◽  
Lung Hypoplasia ◽  
Late Adolescent ◽  
Left Hemithorax ◽  
Rare Case Report

Pulmonary hypoplasia is a bronchopulmonary foregut anomaly in which gross morphology of the lung is preserved but there is decrease in the number or size of airways, vessels, and alveoli. Unilateral pulmonary hypoplasia is a rare clinical condition and most patients reported in the literature are newborns and infants, but patients may remain asymptomatic until late adolescent or till adulthood 65 years old male with parkinsonism was referred to our department with complaints of recent chest symptoms. Clinical examination revealed loss of lung volume in left hemithorax. CT scan thorax and bronchoscopy confirmed the diagnosis of left sided pulmonary hypoplasia. This case report highlights the possibility of pulmonary hypoplasia as one of the differential diagnoses in adult patients presenting with loss of lung volume and to the best of our knowledge he is the eldest patient so far reported.

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 Heart failure presented with massive pleural effusion and mediastinal lymphadenopathy: a rare case report

2014 ◽  
Vol 24 (2) ◽  
pp. 86-88
Author(s):  
Mohammad Shahidul Islam ◽  
Humayara Tabassum ◽  
Sharah Jahan ◽  
Mohammad Shahin Masud ◽  
Muhammad Al Amin ◽  
...  
Keyword(s):  
Heart Failure ◽  
Case Report ◽  
Pleural Effusion ◽  
Ct Scan ◽  
Rare Case ◽  
Unusual Case ◽  
Mediastinal Lymphadenopathy ◽  
Common Cause ◽  
Massive Pleural Effusion ◽  
Rare Case Report

Heart failure may present with diverse manifestation. It is far most common cause of bilateral transudative pleural effusion. In very unusual case, it may present with only massive transudative pleural effusion without cardiomegaly and other features of heart failure such as leg odema, tender hepatomegaly or congested liver. We presented a case that present with massive transudative pleural effusion with mediastinal lymphadenopathy evidenced by CT scan of chest and treated successfully with diuretics. DOI: http://dx.doi.org/10.3329/bjmed.v24i2.20223 Bangladesh J Medicine 2013; 24 : 86-88

scholarly journals Isolated Retrobulbar Orbital Hydatid Cyst: A Rare Case Report

2013 ◽  
Vol 12 (2) ◽  
pp. 220-223
Author(s):  
Kaleem Ahmad ◽  
Sajid Ansari ◽  
Mukesh Kumar Gupta ◽  
RK Rauniyar ◽  
Mohammed Azfar Siddiqui
Keyword(s):  
Case Report ◽  
Hydatid Cyst ◽  
Ct Scan ◽  
Rare Case ◽  
Medical Science ◽  
Surgical Excision ◽  
Rare Manifestation ◽  
Rare Case Report

Isolated orbital hydatid cyst is a rare manifestation most commonly situated in superomedial and superolateral angles of orbit. We report a case of a 24 years old female with a large retrobulbar orbital hydatid cyst causing proptosis which was not associated with any cyst in other organs. USG and CT scan aids to diagnosis while surgical excision and histopathology confirms the diagnosis. Bangladesh Journal of Medical Science Vol. 12 No. 02 April’13 Page 220-223 DOI: http://dx.doi.org/10.3329/bjms.v12i2.14976

scholarly journals Cavernous haemangioma of spleen: a rare case report

2015 ◽  
pp. 2132-2134
Author(s):  
Manjiri Makde ◽  
Roma Rajdeo ◽  
Pradeep Umap ◽  
Anuradha Shrikhande
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Cavernous Haemangioma ◽  
Rare Case Report

scholarly journals Cavernous lymphangioma of eyelid - a rare case report

1970 ◽  
Vol 3 (2) ◽  
pp. 196-198
Author(s):  
Sanjiv Kumar ◽  
Sandeep Kumar ◽  
VK Malik ◽  
K Jain ◽  
C Jain ◽  
...  
Keyword(s):  
Case Report ◽  
Key Words ◽  
Male Patient ◽  
Rare Case ◽  
Lymphatic Malformation ◽  
Lymph Vessels ◽  
Rare Case Report ◽  
Key Words Lymphangioma

Background: Lymphangioma is a lymphatic malformation, a benign proliferation of lymph vessels. Case: We hereby present a case of eyelid lymphangioma of cavernous type in a twelve year old male patient. This is a very uncommon site for this type of lymphangioma. Key words: lymphangioma, eyelid, cavernous type DOI: http://dx.doi.org/10.3126/nepjoph.v3i2.5278 Nepal J Ophthalmol 2011; 3(2): 196-198  

scholarly journals Urinary Bladder Leiomyoma: A Rare Case Report

1970 ◽  
Vol 2 (2) ◽  
pp. 70-71
Author(s):  
HU Bhuiyan
Keyword(s):  
Case Report ◽  
Urinary Bladder ◽  
Key Words ◽  
Female Patient ◽  
Rare Case ◽  
Excision Biopsy ◽  
Key Words Urinary Bladder ◽  
Rare Case Report ◽  
Bladder Leiomyoma

A rare case of urinary bladder leiomyoma in a female patient is presented here. A quarter of these cases are asymptomatic only to be diagnosed by ultrasonography. Symptomatic cases are also misleading as in this case. Laparotomy, removal of mass and ultimately histopathology proved the case to be that of a urinary bladder leiomyoma. Ibrahim Med. Coll. J. 2008; 2(2): 70-71 Key Words: Urinary bladder leiomyoma, laparotomy, excision biopsy doi: 10.3329/imcj.v2i2.2943

scholarly journals Optic Nerve Tortuosity in Neurofibromatosis Type 1: A Rare Case Report

2020 ◽  
pp. 1-4
Author(s):  
Dilek Top Karti ◽  
Omer Karti ◽  
Ali Murat Koç ◽  
Neşe Çelebisoy
Keyword(s):  
Case Report ◽  
Optic Nerve ◽  
Neurofibromatosis Type 1 ◽  
Rare Case ◽  
Neurofibromatosis Type ◽  
Rare Case Report

Inguinal Lymphatic Malformation: A Rare Case Report

2013 ◽  
Vol 12 (3) ◽  
pp. 62-63
Author(s):  
Musrat Rahman ◽  
SAM Alim ◽  
Morsheda Akhter ◽  
Shahana Sultana
Keyword(s):  
Case Report ◽  
Microscopic Examination ◽  
Rare Case ◽  
Cystic Hygroma ◽  
Lymphatic Malformation ◽  
Preoperative Imaging ◽  
Medical College ◽  
Hospital Medical ◽  
Rare Case Report ◽  
The Right

Lymphatic malformation are most commonly located in regions of confluence of major lymphatic channels, including the neck ( 75%), axilla ( 20%), mediastinum, retroperitoneum, pelvis and groin. We are reporting here a very rare case in which a 15 months old boy presented with a painless lump in the right groin. Preoperative imaging, exploration, macroscopic and microscopic examination of the excised specimen revealed it a case of lymphatic malformation (cystic hygroma). This case is unique in terms of site of presentation. Chattagram Maa-O-Shishu Hospital Medical College Journal Volume 12, Issue 3, September 2013: 62-63

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