scholarly journals A rare cause of recurrent gastrointestinal bleed: Blue rubber bleb nevus syndrome

2021 ◽  
Vol 73 ◽  
pp. 352-354
Author(s):  
Jatin Agrawal ◽  
Ashish Kumar ◽  
Anil Arora

Congenital venous malformations (VMs) are rare cause of gastrointestinal (GI) bleed in children. Blue rubber bleb nevus syndrome characterized by VMs in GI tract and skin affect at early age in life. Diagnosis is based on typical skin lesion and history of recurrent GI bleed. In this article, we presented a similar case of young girl with typical skin lesion and recurrent GI bleed requiring multiple blood transfusions presenting our department. She was subjected to surgical treatment and endoscopy therapy due to failure of conservative therapy. This case report depicts importance of typical clinical features of rare diseases.

2021 ◽  
Vol 14 (10) ◽  
pp. e245733
Author(s):  
Guido Gabriele ◽  
Simone Benedetti ◽  
Fabiola Rossi ◽  
Paolo Gennaro

Odontogenic choristomas are a rare and recently classified entity, defined as neoplasms containing tissues of odontogenic derivation, found in abnormal locations and usually diagnosed in the early age. The authors report a unique case of a 79-year-old patient who presented to our attention for a skin lesion in the right cheek with no history of trauma or recent dental procedures, that underneath presented an indolent tooth-like structure inside the soft tissue of the right cheek, which at the histological study resulted to be an odontogenic choristoma. This rare histopathological diagnosis should be considered when a hard lesion is present in the head and neck region.


2020 ◽  
Vol 14 (1) ◽  
pp. 186-196
Author(s):  
Ahmed Ahmed ◽  
Umair M. Nasir ◽  
Paul Delle Donna ◽  
Vanessa Swantic ◽  
Shahida Ahmed ◽  
...  

Lung cancer is a common malignancy which is frequently found to metastasize to distant sites including bone, liver, and adrenal glands. There are rare reports of metastases to the gastrointestinal (GI) tract, with the duodenum being the most uncommon. We present a rare case of a poorly differentiated lung carcinoma metastasizing to the duodenum. This case enhances the medical literature as it provides additional distinct features to the clinical and histological presentation of metastatic lung carcinoma to the GI tract. A 61-year-old male with a history of poorly differentiated lung carcinoma presented with worsening dizziness, fatigue, and early satiety. He had extensive workup done in the past for hemoptysis including a computerized tomography scan of the chest which showed a new lobulated, apical lesion and hilar lymphadenopathy. He ultimately had a transthoracic fine-needle aspiration (FNA) of the mass and was later diagnosed with poorly differentiated lung carcinoma. On examination, the patient was noted to be pale, tachycardic, and hypotensive. The patient was noted to have an acute drop in his hemoglobin requiring fluid resuscitation, multiple blood transfusions, and evaluation with an esophagogastroduodenoscopy. He was found to have an oozing ulcer in the third portion of the duodenum whose biopsies showed poorly differentiated carcinoma with areas of neuroendocrine differentiation, similar to his lung biopsy results, which was consistent with metastatic lung carcinoma.


2016 ◽  
Vol 20 (1) ◽  
Author(s):  
Shalendra Misser

A 40 year old lady had a CT and an MRI scan of her brain for investigation of severe headache following recent recurrent bowel surgery. The post-operative course was complicated by abdominal wall haematoma and she required multiple blood transfusions. Background history of multiple previous bowel resections and chronic anti-inflammatory therapy for inflammatory bowel disease was noted.


Author(s):  
Christine U. Lee ◽  
James F. Glockner

68-year-old man with a history of polycythemia vera and a recent episode of pancreatitis, which required endoscopic drainage of a pancreatic pseudocyst with a cystogastrostomy tube Coronal SSFSE (Figure 5.16.1) and axial fat-suppressed FSE T2-weighted (Figure 5.16.2) images show splenomegaly with a cyst in the posterior spleen. Note also the decreased signal intensity in the liver and spleen due to hemosiderosis from multiple blood transfusions. A round structure in the splenic hilum is bright on T2-weighted images and is surrounded by a small amount of fluid containing a fluid-fluid level. Axial arterial phase and portal venous phase postgadolinium 3D SPGR images (...


2017 ◽  
Vol 86 (1) ◽  
pp. 81
Author(s):  
Paweł Siwiński ◽  
Aleksandra Sobolewska-Włodarczyk ◽  
Marcin Włodarczyk ◽  
Krystyna Stec-Michalska ◽  
Maria Wiśniewska-Jarosińska

Blue rubber bleb nevus syndrome (BRBNS) is an uncommon condition presenting with multiple cutaneous and visceral vascular malformations, predominantly in the gastrointestinal (GI) tract. Typical skin lesion consists of a blue, soft tumor of a rubber like cohesiveness, that is easily compressible and refills slowly on release of pressure. The GI lesions are more clinically relevant, as they may induce chronic bleeding or even life threatening massive hemorrhages. This report presents a case of BRBNS diagnosed in a 52-year-old male with signs of lower gastrointestinal bleeding. The patient presented with melena, fatigue and severe anemia, which were treated by numerous blood transfusions and iron supplementation. Multiple vascular changes were visualized in the small intestine. A typical skin lesion was also present in the skin. Additionally, this report describes the clinical aspects of the syndrome, diagnostic preferences, as well as possible critical complications.


2020 ◽  
Vol 14 (3) ◽  
pp. 467-471
Author(s):  
Eric E. Tibesar

Heterotopic gastric tissue can be found throughout the intestinal tract, and when it is present in the small intestine, it can present with symptoms that include gastrointestinal bleeding, chronic abdominal pain, diarrhea, and chronic dyspepsia. This finding is incredibly rare in pediatrics, but if present, it can lead to significant morbidity and mortality. This can be especially true if a patient presents with a comorbidity of a bleeding disorder. We here present the case of a teenage male with a history of severe factor VII deficiency who was found to have iron deficiency anemia resulting in multiple blood transfusions from an occult lower gastrointestinal bleed. He was ultimately found to have a bleeding gastric heterotopic polyp in his duodenum that was successfully removed via surgery.


2021 ◽  
Vol 36 (2) ◽  
pp. e253-e253
Author(s):  
Abheek Sil ◽  
Dibyendu Bikash Bhanja ◽  
Sayantani Chakraborty

A 36-year-old male presented with multiple red spots over the tongue that appeared at the age of 10 years. In the past two decades, he had suffered from recurrent spontaneous episodes of profuse bleeding from the nose and tongue lesions, requiring hospitalization with multiple blood transfusions. He also complained of exertional breathlessness, easy fatigability, palpitations, and frequent blackouts for the same duration. There was no associated bleeding gums, abdominal pain, melena, seizures, visual disturbances, or hemoptysis. His recently deceased elder brother (in a road traffic accident) had similar mucocutaneous lesions and a history of occasional nose bleeding since adolescence. Their father, too, had non-traumatic epistaxis episodes and died at a young age due to severe hematemesis.


2017 ◽  
Vol 8 (4) ◽  
pp. 24 ◽  
Author(s):  
Emrah Aydin ◽  
Ömer Faruk Beşer

Eosinophilic esophagitis is a chronic disease with immunoallergic etiology. In this condition infiltration of the esophagus with eosinophils, results in esophageal dysfunction. A sixteen years old girl was admitted to the emergency department with profuse hematemesis. Patient needed multiple blood transfusions. Endoscopy ruled out surgical causes of upper GI bleed and esophageal punch biopsy revealed eosinophilic esophagitis. Patient responded well to anti-allergic treatment.


2019 ◽  
Vol 22 (2) ◽  
pp. 32-34
Author(s):  
Kartikesh Mishra

Duodenal adenocarcinoma constitutes 0.4% of gastrointestinal malignancies. Achalasia incidence rate is 0.5-1.2 per 100000. The combination is rare. This is a report of a 68-year-old male from Nepal with history of five years abdominal pain, dysphasia and weight loss. Duodenoscopy could confirm ulcero-proliferative growth at D1-D2. Barium meal depicted features of achalasia cardia. No similar case report suggests that occurrence of duodenal carcinoma and achalasia cardia is merely co- incidental. Discussion: No similar case report suggests that occurrence of duodenal carcinoma and achalasia cardia is merely co- incidental. Consent: Informed consent was obtained from the patient for publication of this case report .


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