Recurrent Esthesioneuroblastoma Presenting as an ACTH Paraneoplastic Syndrome

10.5580/2b51 ◽  
2012 ◽  
Vol 8 (1) ◽  
Keyword(s):  
Paraneoplastic Syndrome

VIP-INDUCED SECRETORY DIARRHEA AS A RARE PARANEOPLASTIC SYNDROME IN CHILDREN WITH NEUROGENIC TUMORS

2020 ◽  
Vol 99 (4) ◽  
pp. 243-251 ◽  
Author(s):  
N.G. Uskova ◽  
◽  
T.V. Shamanskaya ◽  
D.G. Akhaladze ◽  
N.N. Merkulov ◽  
...  
Keyword(s):  
Paraneoplastic Syndrome ◽  
Secretory Diarrhea ◽  
Neurogenic Tumors

Neutrophilic Dermatosis of Hands as Oncological Finding: Importance of Follow-Up

ORL ◽  
2021 ◽  
pp. 1-3
Author(s):  
Jérôme R. Lechien ◽  
Daphné Delplace ◽  
Mohamad Khalife ◽  
Sven Saussez
Keyword(s):  
Head And Neck Cancer ◽  
Head And Neck ◽  
Neck Cancer ◽  
Paraneoplastic Syndrome ◽  
Tobacco Consumption ◽  
Neutrophilic Dermatosis ◽  
Pharyngeal Cancer ◽  
Head And Neck Malignancy ◽  
Neck Malignancy

Neutrophilic febrile dermatosis (NFD) is a rare paraneoplastic syndrome that may be found in patients with head and neck cancer. NFD may appear before the neoplasia and may only concern the dorsal faces of the hands. This article reports the NFD findings of a patient with pharyngeal cancer, which was developed 2 years after the occurrence of NFD. The development of NFD in patient with alcohol and tobacco consumption should lead otolaryngologists and dermatologists to suspect head and neck malignancy. In cases of normal otolaryngological examination, patients have to be followed.

Adrenal Insufficiency as a Paraneoplastic Syndrome in Gastric Adenocarcinoma

2015 ◽  
Vol 47 (4) ◽  
pp. 429-431
Author(s):  
Bilal Farooqi ◽  
Hemant Goyal ◽  
Harold Katner
Keyword(s):  
Adrenal Insufficiency ◽  
Gastric Adenocarcinoma ◽  
Paraneoplastic Syndrome

scholarly journals Cutaneous vasculitis as a paraneoplastic syndrome in adults

1998 ◽  
Vol 41 (6) ◽  
pp. 1133-1135 ◽  
Author(s):  
Carlos Garc�a-Porr�a ◽  
Miguel A. Gonz�lez-Gay
Keyword(s):  
Paraneoplastic Syndrome ◽  
Cutaneous Vasculitis

scholarly journals Paraneoplastic polymyositis presenting as a clinically occult breast cancer

2017 ◽  
Vol 99 (2) ◽  
pp. e40-e43 ◽  
Author(s):  
N Merali ◽  
M Yousuff ◽  
V Pronisceva ◽  
A Poddar
Keyword(s):  
Paraneoplastic Syndrome ◽  
Rare Case ◽  
Primary Tumour ◽  
Imaging Studies ◽  
Occult Breast Cancer ◽  
Symptom Stability ◽  
Underlying Malignancy ◽  
Neurological Presentation ◽  
Complete History ◽  
Metaplastic Breast Carcinoma

Paraneoplastic syndrome affects less than 1% of cancer patients. Diagnosis of paraneoplastic syndrome with neurological presentation requires screening for an underlying malignancy, including a complete history, physical examination and imaging studies. Treatment often results in symptom stability, rather than improvement. Paraneoplastic polymyositis can precede or instantaneously occur at diagnosis or treatment of a primary tumour, while neurological symptoms can persist even following cancer treatment. We report a rare case of metaplastic breast carcinoma with an unusual presentation of paraneoplastic polymyositis.

Commentary: Paraneoplastic Syndrome Associated with Kelch‐Like Protein 11 Antibodies Presenting with Progressive Ataxia and Tremor

2021 ◽  
Vol 8 (S1) ◽  
Author(s):  
Alfonso Fasano ◽  
Prarthana Prakash ◽  
Ian O. Bledsoe ◽  
Bettina Balint
Keyword(s):  
Paraneoplastic Syndrome ◽  
Progressive Ataxia

Granulocytosis, a Paraneoplastic Syndrome Associated With Non-Glandular Squamous Cell Carcinomas (NGSCC) in the Tg.rasH2 Studies

2021 ◽  
pp. 019262332110557
Author(s):  
Madhav Paranjpe ◽  
Peter Mann ◽  
Melissa Denton
Keyword(s):  
Squamous Cell Carcinoma ◽  
Cell Carcinoma ◽  
Squamous Cell ◽  
Paraneoplastic Syndrome ◽  
Statistical Significance ◽  
Squamous Cell Carcinomas ◽  
Rare Tumor ◽  
Male Mice ◽  
Control Male ◽  
Control Female

Non-glandular squamous cell carcinoma (NGSCC) is an extremely rare tumor in Tg.raH2 mice. There have been 5 NGSCC in 1615 control male mice (0.31%) and 2 NGSCC in 1560 control female mice (0.13%) on 26-week carcinogenicity studies, with a range of 0 to 1 of per group per sex in each study without statistical significance in 52 male and 51 female studies conducted in Tg.rasH2 mice. Every case of NGSCC was accompanied by profound granulocytosis.

scholarly journals Necrotizing leptomeningeal vasculitis associated with a compressive meningioma in a cat: a rare paraneoplastic syndrome

2012 ◽  
Vol 2 (1) ◽  
pp. 4
Author(s):  
Les J. Gabor ◽  
Ines Walther ◽  
Kathleen Mullins ◽  
Melinda Gabor ◽  
Andrea Borque
Keyword(s):  
Paraneoplastic Syndrome ◽  
Necrotizing Vasculitis ◽  
First Report ◽  
Domestic Species

A 17 year old cat with a compressive meningioma was found to have an intradural, severe necrotizing vasculitis, spatially un associated with the neoplasm. Paraneoplastic vasculitis has been reported in two cases in the human literature associated with meningiomas. This is the first report of such an association in a domestic species.

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