581: A RARE CASE OF HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS (HLH) DUE TO PRIMARY ADRENAL LYMPHOMA

2018 ◽  
Vol 46 (1) ◽  
pp. 276-276 ◽  
Author(s):  
Amar Jadhav ◽  
David Tannehill
2018 ◽  
Author(s):  
Maria Mavromati ◽  
Olivier Nawej ◽  
Olga Tsopra ◽  
Heba Al-Alwan ◽  
Francois Jornayvaz ◽  
...  

2020 ◽  
Vol 5 (1) ◽  
Author(s):  
Tara S Kim ◽  
Kwan Cheng ◽  
Radhika Jaiswal ◽  
Pranisha Gautam-Goyal ◽  
Alyson K Myers

Abstract Adrenal incidentalomas, masses noted on imaging performed for other purposes, are common, with 10% to 15% presenting as bilateral adrenal masses. These cases can be challenging as the differential diagnosis is broad, including metastatic disease, primary adrenal lymphoma (PAL), or infection, and often requiring a biopsy if initial biochemical workup is unrevealing. We present here a relevant case description, laboratory and radiologic imaging studies, and discussion of literature. A 62-year-old Korean woman presented with altered mental status and fevers. She was found to have bilateral adrenal incidentalomas and retained acupuncture needles. Adrenal workup did not show biochemical evidence of hormonal excess. Infectious workup was unrevealing, as was a metal/toxin workup due to retained acupuncture needles. Fevers and episodes of hypotension persisted which prevented the patient from obtaining an adrenal biopsy. Bone marrow biopsy was obtained for pancytopenia and revealed B-cell lymphoma with large cell morphology and few histiocytes with hemophagocytosis, raising concern for lymphoma-induced hemophagocytic lymphohistiocytosis (HLH). PAL associated with HLH was highly suspected in our patient, given the large (7 cm) bilateral adrenal masses and bone marrow biopsy findings of lymphoma. The patient was treated for diffuse large B-cell lymphoma, with clinical improvement. PAL is a rare but aggressive lymphoma with few reported cases. It should be considered in the differential for both unilateral and bilateral adrenal masses. An early diagnosis is crucial as the main treatment is chemotherapy rather than surgery and it confers a significant survival benefit.


Folia Medica ◽  
2021 ◽  
Vol 63 (3) ◽  
pp. 443-447
Author(s):  
Alexey V. Shabunin ◽  
Dmitry N. Grekov ◽  
Ivan N. Lebedinsky ◽  
Andrey I. Evsikov ◽  
Serghei Covantev ◽  
...  

Adrenal gland incidentaloma (incidental – sudden, accidental) is a mass of the adrenal gland(s), accidentally detected by an instru-mental examination conducted for other reasons. The frequency of detection of this pathology based on computer tomography of the abdominal organs is 0.5%–2%. In most cases, the mass is represented by adrenocortical adenomas without hormonal secretion. It is an extremely rare case (less than 1% of all cases) when the adrenal incidentaloma is a primary adrenal lymphoma, which accounts for 1% of all non-Hodgkin lymphomas and 3% of all extranodal lymphomas with a few cases reported in the literature. In our article, we present a case of left adrenal incidentaloma of the adrenal gland, which, during further observation and examination, increased in size, which was the reason for performing laparoscopic adrenalectomy. According to the results of the histological examination, the mass turned out to be diffuse large B-cell lymphoma.


2019 ◽  
Author(s):  
Medine Nur Kebapci ◽  
Arzu Dağdemir ◽  
Aysen Akalın ◽  
Mahmut Kebapci ◽  
Funda Canaz

2005 ◽  
Vol 15 (6) ◽  
pp. 340-342 ◽  
Author(s):  
Pinaki Dutta ◽  
Anil Bhansali ◽  
Rajarajan Venkatesan ◽  
Bhagwant Rai Mittal ◽  
Vijay Kumar

Cureus ◽  
2020 ◽  
Author(s):  
Theano Lagousi ◽  
Paraskevi Korovessi ◽  
Eleni Panagouli ◽  
Vasilis Tsagris ◽  
Stavroula Kostaridou

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