scholarly journals Recurrent chest pain as a rare presentation of extra-pelvic endometriosis

Author(s):  
Mousa Hussein ◽  
Mutaz Al bakri ◽  
Shanima Ismail ◽  
Abbas Alabbas ◽  
Sameer Alhyassat

Periodic chest pain, with bloody pleural effusion, should raise the suspicion of pleural endometriosis as a well-known, but rare condition in clinical practice.

2018 ◽  
Vol 2018 ◽  
pp. 1-4 ◽  
Author(s):  
Muhammad Shabbir Rawala ◽  
Muhammad Farhan Khaliq ◽  
Muhammad Asif Iqbal ◽  
S. Tahira Shah Naqvi ◽  
Kinaan Farhan ◽  
...  

Endometriosis is a common condition in which endometrial cells and stroma are deposited in extrauterine sites. Its prevalence has been estimated to be 10% of reproductive age females. It is commonly found in the pelvis; however, it may be found in the abdomen, thorax, brain, or skin. Thoracic involvement is a relatively rare presentation of this common disease. Thoracic endometriosis commonly presents as pneumothorax in 73% of patients. A rarer presentation of thoracic endometriosis is hemothorax (<14%) or hemoptysis (7%). Thoracic endometriosis is an uncommon cause of a pleural effusion. We present a case of 28-year-old African American female with no other medical conditions. She presented to the hospital with worsening right-sided pleuritic chest pain, dyspnea, and menorrhagia. She had been complaining of pleuritic chest pain for 5 years, the onset of which corresponds to the start of her menstrual cycle and is relieved with cessation of menses. Initial laboratory studies revealed a severe microcytic anemia with normal coagulation profile. Chest X-ray showed small right pleural effusion and suspicious for airspace disease. A computed tomography (CT) of chest was ordered for further clarification and identified large right pleural effusion. CT-guided thoracentesis removed 500 ml of serosanguinous fluid consisting of blood elements. There can be multiple sites involved with endometriosis and can present with wide range of symptoms that occur periodically with menses in young woman. The history and pleural fluid findings of this case are suggestive of Thoracic Endometriosis Syndrome. The diagnosis of this is often missed or delayed by clinicians, which can result in recurrent hospitalization and other complications. As internists we should be suspicious of atypical presentations of endometriosis and treat them early before complications develop. This case also highlights the importance of suspecting atypical etiologies for pleural effusion.


2021 ◽  
Vol 9 (7) ◽  
Author(s):  
Mousa Hussein ◽  
Mutaz Albakri ◽  
Shanima Ismail ◽  
Abbas Alabbas ◽  
Samir Al Hyassat

2021 ◽  
pp. 4-6
Author(s):  
Michael Tyodoo Maanongun ◽  
Andrea Avershima Ornguze ◽  
Babarinde Ojo

Meigs' syndrome is a rare condition characterized by the presence of a benign broma of the ovary, ascites and pleural effusion. When either of ascites or pleural effusion is associated with the broma it is termed pseudo-Meigs' syndrome. Though bromas are the most common benign solid tumours of the ovary, they rarely present in clinical practice and diagnosis is made difcult by symptoms that usually mimic disseminated malignancy. The gold standard of treatment is laparotomy, denitive diagnosis is by histology, and by denition of the syndrome, the symptoms resolve after removal of the tumour and the patients become asymptomatic. We present a patient with a giant ovarian broma with associated pseudo Meigs syndrome who was successfully managed without any complications.


2011 ◽  
Vol 2 (3) ◽  
pp. 128-130 ◽  
Author(s):  
Mohammad Shameem ◽  
Jamal Akhtar ◽  
Nafees Ahmad Khan ◽  
Ummul Baneen ◽  
Rakesh Bhargava ◽  
...  

2021 ◽  
Vol 14 (11) ◽  
pp. e244616
Author(s):  
Saurabh Kumar ◽  
Arun Paul Charllu

Pseudoankylosis is a rare condition that causes inability to open the mouth due to condition related to outside of the temporomandibular joint. Most literature refers to this hypomobility disorder, a result of fusion of the zygomatic bone to the coronoid process, and very rarely is insidious coronoid hyperplasia causing mechanical interference with the posterior maxilla has been reported. We present a case of a 45-year-old woman, who presented with coronoid malformation and overgrowth resulting in progressive decrease in mouth opening. She was managed with coronoidectomy, following which good mouth opening was obtained. In this paper we discuss about the diagnosis and management of this rare disorder.


2021 ◽  
pp. 17-18
Author(s):  
Tejasvini Chandra ◽  
Perwez Khan ◽  
Lubna Khan ◽  
Anshika Gupta

We report bilateral proptosis as the initial presentation of Acute Myeloid Leukemia (AML) in a child. An Eight year child presented with a history of painless proptosis in the both eyes within 10 days. Radiological investigation (CT scan) showed inltration of orbit with the metastatic tumour cell. AML was diagnosed with complete blood count, General Blood Picture (GBP) and bone marrow biopsy. The presumptive diagnosis of leukemic inltration of the orbit is made. We report this case as AML can rarely present in child as a bilateral proptosis due to leukemic inltration. Urgent treatment modality for this rare condition is radiation.


Thorax ◽  
2010 ◽  
Vol 65 (9) ◽  
pp. 769-769 ◽  
Author(s):  
X. Zhi ◽  
Z. Qiao ◽  
W. Changzheng ◽  
W. Guoming ◽  
W. Guansong ◽  
...  
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