scholarly journals Pulmonary nodular lymphoid hyperplasia presenting as multifocal subsolid nodules: A case report and literature review

2022 ◽  
pp. 101581
Author(s):  
Yoon Jin Cha ◽  
Duk Hwan Moon ◽  
Ji Hyun Park ◽  
Sungsoo Lee ◽  
Ji Ae Choi ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymphoid Hyperplasia ◽  
Nodular Lymphoid Hyperplasia

Benign Lymphoid Hyperplasia of the Tongue Masquerading as Carcinoma: Case Report and Literature Review

2005 ◽  
Vol 6 (3) ◽  
pp. 111-119 ◽  
Author(s):  
Sunitha Carnelio ◽  
Gabriel Rodrigues
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymphoid Hyperplasia ◽  
Germinal Centers ◽  
Major Surgery ◽  
Benign Lymphoid Hyperplasia ◽  
Mononuclear Infiltrate ◽  
Carcinoma Of The Tongue

Abstract Lymphoid hyperplasia of the tongue is a very rare benign lymphoproliferative lesion that closely resembles carcinoma or lymphoma, clinically or histopathologically. A case of benign lymphoid hyperplasia (BLH) of the tongue is reported. Clinically this lesion presented as a painless ulcer, which mimicked carcinoma of the tongue. Microscopy showed typical histologic features of multiple germinal centers with a rim of small mature lymphocytes together with a mixed, mainly mononuclear infiltrate which clinched the diagnosis of benign lymphoid hyperplasia. This diagnosis averted extensive investigations and major surgery. The etiology of these lesions is unknown. Their distinction from carcinoma and lymphoma is discussed. Citation Carnelio S, Rodrigues G. Benign Lymphoid Hyperplasia of the Tongue Masquerading as Carcinoma: Case Report and Literature Review. J Contemp Dent Pract 2005 August;(6)3:111-119.

scholarly journals Pediatric Covid-19 mesenteric lymphoid hyperplasia associated intussusception: A case report and literature review

2021 ◽  
Vol 73 ◽  
pp. 101988
Author(s):  
Shahfar Khan ◽  
Luke Hartman ◽  
Youck Jen Siu Navarro ◽  
Connie J. Rossini ◽  
Catherine Burdett ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymphoid Hyperplasia

Dasatinib-associated follicular lymphoid hyperplasia: First pediatric case report and literature review

2017 ◽  
Vol 64 (11) ◽  
pp. e26597 ◽  
Author(s):  
Emilie Bouquet ◽  
Anne Jourdain ◽  
Marie-Christine Machet ◽  
Frédérique Beau-Salinas ◽  
Annie-Pierre Jonville-Béra
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymphoid Hyperplasia ◽  
Pediatric Case

P.05.12 DIFFUSE INTESTINAL NODULAR LYMPHOID HYPERPLASIA (DNLH) IN A PATIENT WITH EPIGASTRIC PAIN: A CASE REPORT

2016 ◽  
Vol 48 ◽  
pp. e152
Author(s):  
E. Capoferro ◽  
E. Ntakirutimana ◽  
D. Dal Fior ◽  
R. Colombari ◽  
P. Inturri ◽  
...  
Keyword(s):  
Case Report ◽  
Epigastric Pain ◽  
Lymphoid Hyperplasia ◽  
Nodular Lymphoid Hyperplasia

Follicular lymphoid hyperplasia of the palate: Case report and literature review

2009 ◽  
Vol 37 (2) ◽  
pp. 79-82 ◽  
Author(s):  
Bruno C. Jham ◽  
Nada O. Binmadi ◽  
Mark A. Scheper ◽  
Xianfeng F. Zhao ◽  
Gary E. Koterwas ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Lymphoid Hyperplasia

scholarly journals Case Report: Intestinal Nodular Lymphoid Hyperplasia as First Manifestation of Activated PI3Kδ Syndrome Due to a Novel PIK3CD Variant

2021 ◽  
Vol 9 ◽  
Author(s):  
Antonio Marzollo ◽  
Silvia Bresolin ◽  
Davide Colavito ◽  
Alice Cani ◽  
Paola Gaio ◽  
...  
Keyword(s):  
Case Report ◽  
Complete Remission ◽  
Clonal Expansion ◽  
Lymphoid Hyperplasia ◽  
Lymphoproliferative Disease ◽  
Lymphoid Cells ◽  
The Novel ◽  
First Line ◽  
Nodular Lymphoid Hyperplasia ◽  
Gut Mucosa

Nodular lymphoid hyperplasia (NLH) is a lymphoproliferative disease caused by non-clonal expansion of lymphoid cells in the gut mucosa. Little is known about the pathogenesis of NLH, which is often disregarded as an insignificant or para-physiologic phenomenon. We present the case of a girl with isolated diffuse NLH (extending from the stomach to the rectum) caused by activated PI3Kδ syndrome (APDS) due to the novel p.Glu525Gly variant in PIK3CD. The gain-of-function effect of the variant was confirmed by demonstration of over activation of the Akt/mTOR pathway in the patient's cells. APDS diagnosis led to treatment with sirolimus, which resulted in the complete remission of NLH and in the prevention of extra intestinal complications. In conclusion, we identify APDS as a novel cause of isolated NLH and suggest that patients with severe pan-enteric NLH should be screened for this disorder that may not be apparent on first-line immunological testing.

Reactive lymphoid hyperplasia of liver mimicking late ovarian cancer recurrence: case report and literature review

2011 ◽  
Vol 16 (6) ◽  
pp. 714-717 ◽  
Author(s):  
Claudia Marchetti ◽  
Natalina Manci ◽  
Marco Di Maurizio ◽  
Chiara Di Tucci ◽  
Moira Burratti ◽  
...  
Keyword(s):  
Ovarian Cancer ◽  
Case Report ◽  
Literature Review ◽  
Cancer Recurrence ◽  
Lymphoid Hyperplasia ◽  
Reactive Lymphoid Hyperplasia
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