A rare presentation of plasmablastic lymphoma as cutaneous nodules in an immunocompromised patient

2016 ◽  
Vol 28 (6) ◽  
pp. 623-625 ◽  
Author(s):  
Selvin Sundar Raj Mani ◽  
Thomas Kodiatte ◽  
Manjeera Jagannati

Plasmablastic lymphoma is a rare entity accounting for around 2.7% of all AIDS-related lymphomas. The oral cavity and gastrointestinal tract are the most common sites involved. We report a case of a 34-year-old HIV-positive woman with a rare presentation of cutaneous nodules all over the body. Due to overwhelming tumour burden, she developed tumour lysis syndrome during her hospital stay and succumbed to the illness.

2011 ◽  
Vol 52 (9) ◽  
pp. 970-972 ◽  
Author(s):  
William Makis ◽  
Anthony Ciarallo ◽  
Robert Lisbona

Plasmablastic lymphoma of the oral cavity is a very rare and only recently recognized entity that has been identified almost exclusively in HIV-infected individuals. It has a predilection for the oral cavity, often exhibits very aggressive behavior and has a poor prognosis. The use of 18F-FDG PET/CT in the evaluation of HIV-associated lymphomas is a recent development, and its use in the staging of plasmablastic lymphoma of the oral cavity has not been previously reported. This rare report highlights the usefulness of 18F-FDG PET/CT in the staging of plasmablastic lymphoma of the oral cavity.


2020 ◽  
Vol 10 (5) ◽  
pp. 183-184
Author(s):  
Rafael Ferreira Nascimento ◽  
Diogo Raposo André, ◽  
Fabiana Gouveia ◽  
Nancy Faria ◽  
Ana Paula Reis

Introduction: The authors describe a rare presentation of central nervous system cryptococcosis in an immunocompromised patient. Case description: An HIV-positive patient, with poor adherence to the treatment, presented with a seventeen days history of severe headache. On the neurological exam there was only evidence of neck stiffness, he had a CD4 count of 23 cells/μl and plasma HIV RNA viral loads of 364,000 copies/ml. Lumbar puncture revealed positive for cryptococcal antigen virus and so treatment with amphotericin B was started. During his admission the patient developed an expressive aphasia with visual hallucinations and the brain MRI revealed cerebral cryptococcomas. After 98 days of treatment general and neurological examination was normal and the patient was discharged home. Conclusion: This case highlights a rare and severe complication of Cryptococcus neoformans infection in immunocompromised patients.


Oral Surgery ◽  
2015 ◽  
Vol 8 (4) ◽  
pp. 232-237
Author(s):  
O. Tabbenor ◽  
T. Halai ◽  
E. Bailey ◽  
P. Coulthard

2018 ◽  
Vol 2018 ◽  
pp. 1-3
Author(s):  
A. Moramarco ◽  
M. Marenco ◽  
M. La Cava ◽  
A. Lambiase

Plasmablastic lymphoma (PBL) is a malignant, rare, and aggressive form of non-Hodgkin’s lymphoma with poor response to treatment that most commonly involves the oral mucosa of immunodeficient patients. The orbit might be primarily or secondarily involved; on the other hand other pathological conditions, i.e., fungal infections, may localize in the orbit in both immunocompromised patients and drug user, which might have similar radiological features. We describe the clinical, radiological, and pathological features of an orbital plasmablastic lymphoma (PBL) in an immunocompromised HIV positive drug user patient.


2019 ◽  
Vol 12 (3) ◽  
pp. e227510
Author(s):  
Cláudia Santos ◽  
Ana Virgínia Araújo ◽  
Helena Contente ◽  
Cláudia Branco

Granular cell tumours are rare neoplasms that may occur anywhere in the body. The most common locations are the oral cavity, skin and subcutaneous tissue, with only 8% of these tumours occurring at a gastrointestinal site. In the specific case of gastric granular cell tumours, only a few cases have been published until today. Granular cell tumours are usually benign; however, some malignant forms have been reported. Both endoscopic and surgical resection represent the treatment of choice. The authors report a new clinical case of a gastric granular cell tumour, treated with laparoscopic surgical resection, describing some endoscopic, imagiological and anatomopathological features.


Author(s):  
Raghu Radhakrishnan ◽  
Setty Suhas ◽  
Rekha V. Kumar ◽  
Geeta Krishnanand ◽  
Rangarajan Srinivasan ◽  
...  

1995 ◽  
Vol 9 (1) ◽  
pp. 43-48 ◽  
Author(s):  
Jonathan A. Lesserson ◽  
Douglas G. Finn

Amyloidosis of the nasopharynx is a rare presentation of localized amyloidosis. The majority of systemic amyloidosis cases involve the heart, gastrointestinal tract, kidneys, and upper and lower respiratory tract. Localized amyloidosis involving only one site is less common, but has been observed in the head and neck area, particularly in the larynx or the oral cavity. Amyloidosis in the nasopharynx has been reported in only seven previous cases in the English literature.


2015 ◽  
pp. bcr2015211960
Author(s):  
Sidhertha Podder ◽  
Prerna Khetan ◽  
Shetra Sivamurthy ◽  
Kaushik Mandal

2013 ◽  
Vol 3 (1) ◽  
pp. 28-30
Author(s):  
Vidya Bhushan Rangappa ◽  
Raghavendra Suresh

ABSTRACT Leiomyomas are benign soft tissue neoplasms that arise from smooth muscle. Cases have been reported in the gastrointestinal tract, brain, oral cavity and other sites. Laryngeal angioleiomyomas are infrequently reported. Literature search revealed no case reported in the hypopharynx. We report a case of 40-year-old female with angioleiomyoma of the hypopharynx. External approaches have been described in the literature for laryngeal leiomyomas. We discuss the endolaryngeal approach for removal of these tumors. How to cite this article Suresh R, Balasubramanya AM, Rangappa VB. Angioleiomyoma of the Hypopharynx: A Rare Entity. Int J Phonosurg Laryngol 2013;3(1):28-30.


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