scholarly journals Angiolymphoid hyperplasia with eosinophilia: A rare benign vascular tumor of breast

2013 ◽  
Vol 56 (4) ◽  
pp. 405 ◽  
Author(s):  
Neelima Tirumalasetti
Keyword(s):  
Vascular Tumor ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia

ANGIOLYMPHOID HYPERPLASIA WITH EOSINOPHILIA: A CASE REPORT OF A RARE BENIGN VASCULAR TUMOR

2020 ◽  
Vol 130 (3) ◽  
pp. e174
Author(s):  
RODRIGO PORPINO MAFRA ◽  
LARISSA SANTOS AMARAL ROLIM ◽  
CARLA SAMILY DE OLIVEIRA COSTA ◽  
EVERTON FREITAS DE MORAIS ◽  
HEVIO FREITAS DE LUCENA ◽  
...  
Keyword(s):  
Case Report ◽  
Vascular Tumor ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia

scholarly journals Dilemma in diagnosing a post-auricular mass-angiolymphoid hyperplasia with eosinophilia versus Kimura’s disease, an infrequent encounter

2021 ◽  
Vol 7 (3) ◽  
pp. 544
Author(s):  
Sandeep Shetty ◽  
Shilpa Chandrashekar ◽  
Nivetha Devi Ganesan ◽  
Debayan Dey ◽  
Ramya Sathanur Bhaskarachar
Keyword(s):  
Normal Skin ◽  
Correct Diagnosis ◽  
Inflammatory Cells ◽  
Vascular Tumor ◽  
Chronic Inflammatory Disease ◽  
Kimura’S Disease ◽  
Soft Tissue Neoplasm ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia ◽  
Hrct Temporal Bone

<p class="abstract">Angiolymphoid hyperplasia with eosinophilia (ALHE) and Kimura’s disease are uncommon chronic benign lesions of the skin mainly involving the head and neck regions where ALHE involves vascular and lymphocytic proliferation and Kimura’s is of inflammatory type. Dermal involvement is more in ALHE but In Kimura’s disease the lymphnodes and subcutaneous tissues are involved more. ALHE is a rare vascular tumor and Kimura’s disease is a chronic inflammatory disease. Both not only have uncertainty in etiology and pathogenesis, but also there is therapeutic dilemma in management. In this article, we describe a case of ALHE which presented to our ENT outpatient department with swelling in the left postauricular region which appeared 1.5 years back and posed a riddle in coming to correct diagnosis. On examination, a single smooth spherical swelling in upper part of post-auricular region of size 3×3 cm with well-defined edges and normal skin. Blood investigations revealed elevated absolute eosinophil count. HRCT temporal bone showed a well-defined rounded hypo-dense lesion measuring 28×23 mm with no effect of adjacent bony erosion / calcifications/ cystic changes suggestive of benign etiology. FNAC showed scantly cellular and occasionally scattered fibroblasts, pinkish stromal collagen fragments with inflammatory cells in background of haemorrhage suggestive of soft tissue neoplasm.</p>

Angiolymphoid Hyperplasia with Eosinophilia (Histiocytoid Hemangioma): Evaluation of Treatment Options

1993 ◽  
Vol 102 (4) ◽  
pp. 303-308 ◽  
Author(s):  
Mack L. Cheney ◽  
Samir Bhatt ◽  
Paul Googe ◽  
Patricia L. Hibberd
Keyword(s):  
Treatment Options ◽  
Clinical Problem ◽  
Radical Excision ◽  
Angiolymphoid Hyperplasia With Eosinophilia ◽  
Angiolymphoid Hyperplasia ◽  
Immunodeficiency Virus ◽  
Long Term Follow Up ◽  
Proliferative Lesion

Angiolymphoid hyperplasia with eosinophilia is an uncommon benign vascular proliferative lesion of unknown cause. In this report, a case is presented of a patient who was confirmed to be positive for human immunodeficiency virus and in whom the lesion had shown rapid accelerated growth. The case is used to illustrate a variety of therapeutic techniques and to evaluate the effectiveness of the various alternatives in the treatment of this unusual clinical problem. Long-term follow-up after radical excision of the tumor mass is presented.

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