Reactive Eccrine Syringofibroadenomatosis Associated With Venous Leg Ulcers: A Case Report and Literature Review

2020 ◽  
pp. 153473462096690
Author(s):  
Billal Tedbirt ◽  
Priscille Carvalho ◽  
Claire Boulard ◽  
Florence Tetart ◽  
Aurélie Deschamps-Huvier ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Leg Ulcers ◽  
Histological Features ◽  
Venous Leg Ulcers ◽  
Adnexal Tumor ◽  
Skin Biopsies ◽  
Chronic Leg Ulcers

Eccrine syringofibroadenoma (ESFA) is a rare adnexal tumor deriving from the acrosyringeal portion of the eccrine duct. Five subtypes of ESFA were described including a reactive form. Reactive ESFAs are associated with inflammatory and neoplastic dermatoses. In this article, we report the case of a 90-year-old woman presenting with 3 leg ulcers evolving for 2 years surrounded by large verrucous and eczematous lesions. Multiple skin biopsies showed anastomosing epithelial cords connected to the epidermis consistent with ESFA. We identified 8 cases of ESFA associated with chronic leg ulcers in the literature and reviewed their main clinical and histological features.

Case Report and Literature Review of Nodular Hidradenoma, a Rare Adnexal Tumor That Mimics Breast Carcinoma, in a 20-Year-Old Woman

2019 ◽  
Vol 50 (3) ◽  
pp. 320-325
Author(s):  
Vanya Jaitly ◽  
Richard Jahan-Tigh ◽  
Tatiana Belousova ◽  
Hui Zhu ◽  
Robert Brown ◽  
...  
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Breast Carcinoma ◽  
Literature Review ◽  
Sweat Glands ◽  
Rare Presentation ◽  
Adnexal Tumor ◽  
Nodular Hidradenoma ◽  
Growing Mass ◽  
Uncommon Tumor

Abstract Nodular hidradenoma is an uncommon cutaneous adnexal tumor arising from sweat glands. In the skin, it usually presents as a solitary dermal nodule; excision is curative in most cases. In rare instances, it may present as a breast mass and can mimic breast carcinoma clinically and radiologically, causing diagnostic dilemmas for the treating physician and pathologist. Herein, we discuss a case of nodular hidradenoma in a 20-year-old Hispanic woman as a rapidly growing mass in the breast that mimicked breast carcinoma. We discuss the rare presentation of this uncommon tumor and the differential diagnosis of this entity, as well as the results of our literature review on the topic.

Bullous Pilomatricoma: A Report of Clinical and Pathologic Findings and Review of Dermal Bullous Disorders

2001 ◽  
Vol 5 (5) ◽  
pp. 394-396 ◽  
Author(s):  
Gabriele E. Weichert ◽  
Kevin L. Bush ◽  
Richard I. Crawford
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Unusual Feature ◽  
Nous Rapportons ◽  
Pathological Feature ◽  
Pathological Features ◽  
Pathologic Findings ◽  
Hair Matrix ◽  
Adnexal Tumor ◽  
Vaisseaux Lymphatiques

Background: Pilomatricoma is a common benign adnexal tumor differentiating toward elements of the hair matrix and shaft. It typically presents as a solitary, deep, dermal nodule. We describe a case of a pilomatricoma with the unusual feature of a thick-walled dermal bulla overlying the tumor. Objective: We describe a case of bullous pilomatricoma and discuss the potential etiology of the bullous feature of the lesion. Methods: This article includes a case report and a literature review. Conclusions: Bullous pilomatricoma has rarely been described. A common pathological feature in this type of pilomatricoma is the presence of dilated lymphatics. Bullous morphea associated with dermal lymphatic dilation has also been described. In both bullous pilomatricoma and morphea, it is possible that individual pathological features of the lesion lead to obstruction and congestion of the dermal lymphatics thereby inducing enough dilation and edema to form a dermal bulla. Antécédents: Le pilomatrixome (épithéliome calcifiant de Malherbe) est une tumeur annexielle bénigne qui ressemble aux éléments de la matrice et de la tige pilaires. Il se manifeste typiquement par un nodule sous-cutané solitaire. Nous rapportons un cas de pilomatrixome présentant la caractéristique inhabituelle d'une bulle dermique à paroi épaisse située au-dessus de la tumeur. Objectifs: Décrire un cas de pilomatrixome bulleux et présenter l'étiologie potentielle d'une telle manifestation. Méthodes: Cet article comporte une étude de cas ainsi qu'une revue de la littérature. Conclusion: Le pilomatrixome bulleux a rarement été décrit. La dilatation des vaisseaux lymphatiques constitue une manifestation pathologique fréquente de cette forme de pilomatrixome. La morphée bulleuse a également été associée à une dilatation de vaisseaux lymphatiques. Il est possible que les caractéristiques pathologiques individuelles des lésions du pilomatrixome bulleux et de la morphée entraînent une obstruction et une congestion des vaisseaux lymphatiques, provoquant ainsi une dilatation et un œdème suffisamment importants pour former une bulle.

scholarly journals Meconium periorchitis: A case report and literature review

2013 ◽  
Vol 7 (7-8) ◽  
pp. 495 ◽  
Author(s):  
Ammar Hameed Alanbuki ◽  
Ashwith Bandi ◽  
Nick Blackford
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rare Disease ◽  
Relevant Literature ◽  
Plain Film ◽  
Meconium Peritonitis ◽  
Histological Features ◽  
Abdominal Plain Film ◽  
Scrotal Ultrasound

Meconium periorchitis (MPO) is an uncommon entity associated with healed meconium peritonitis. The typical presentation is a soft hydrocele at birth which becomes harder in weeks as the meconium calcifies. A lack of awareness of this rare disease may lead to unnecessary surgery of scrotal masses. It can resolve spontaneously without compromising the testicle. Scrotal ultrasound is the mainstay of imaging and abdominal plain film is less sensitive but can help in the diagnosis. We report a case of a meconium periorchitis and discuss its radiological and histological features. We also review the relevant literature.

scholarly journals Large Wolffian adnexal tumor of the ovary: A case report and literature review

2017 ◽  
Author(s):  
Ya‑Qiong Du ◽  
Shu‑Zheng Song ◽  
Xiao‑Chun Ni ◽  
Ju‑Gang Wu ◽  
Shou‑Lian Wang ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Adnexal Tumor

scholarly journals Intravascular Large B Cell Lymphoma Presenting as Fever of Unknown Origin and Diagnosed by Random Skin Biopsies: A Case Report and Literature Review

2017 ◽  
Vol 18 ◽  
pp. 482-486 ◽  
Author(s):  
Horacio di Fonzo ◽  
Damian Contardo ◽  
Diego Carrozza ◽  
Paola Finocchietto ◽  
Adriana Rojano Crisson ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
B Cell ◽  
Fever Of Unknown Origin ◽  
Cell Lymphoma ◽  
Unknown Origin ◽  
B Cell Lymphoma ◽  
Large B Cell Lymphoma ◽  
Skin Biopsies ◽  
Large B Cell

scholarly journals Sialolipoma of the Lower Lip: Case Report and Literature Review

2012 ◽  
Vol 6 (1) ◽  
pp. 208-211 ◽  
Author(s):  
Nada O Binmadi ◽  
Risa Chaisuparat ◽  
Bernard A Levy ◽  
Nikolaos G Nikitakis
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Literature Review ◽  
Parotid Gland ◽  
Maxillofacial Region ◽  
Lower Lip ◽  
Histological Features ◽  
Common Location ◽  
Oral And Maxillofacial Region

Sialolipoma is a relatively rare and fairly recently described as a variant of lipoma with salivary elements. Any site within the oral and maxillofacial region may be involved with the parotid gland being the most common location. Herein, we present a case of silaolipoma in lower lip. The clinical and histological features and differential diagnosis are discussed.

Active debridement of venous leg ulcers: a literature review to inform clinical practice

2019 ◽  
Vol 24 (Sup6) ◽  
pp. S24-S29
Author(s):  
Lucy Hall ◽  
Una Adderley
Keyword(s):  
Literature Review ◽  
Research Evidence ◽  
Compression Therapy ◽  
Routine Practice ◽  
Leg Ulcers ◽  
Qualitative And Quantitative ◽  
Venous Leg Ulcers ◽  
Quantitative Studies ◽  
Infection Source ◽  
Robust Evidence

Community nurses often care for patients with sloughy venous leg ulcers. Slough is viewed as a potential infection source and an impediment to healing, but it is unclear if active debridement of slough promotes healing. Using a clinical scenario as a contextual basis, this literature review sought research evidence to answer this clinical question. A strategy based on the ‘4S’ approach was used to identify research evidence. The retrieved evidence included one systematic review, three clinical guidelines and six qualitative and quantitative studies. The analysis suggested that there is no robust evidence to support the routine practice of active debridement of venous leg ulcers to promote healing, and that debridement is associated with increased pain. Since autolytic debridement can be achieved through the application of graduated compression therapy, active debridement may offer no additional benefit.

scholarly journals Primary Adrenal Leiomyosarcoma: A Case Report and Literature Review

2008 ◽  
Vol 2 ◽  
pp. CMO.S627 ◽  
Author(s):  
M Mencoboni ◽  
M Bergaglio ◽  
M Truini ◽  
M Varaldo
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Adrenal Mass ◽  
Clinical Course ◽  
Therapeutic Strategies ◽  
Anatomic Site ◽  
Histological Features ◽  
Mesenchymal Neoplasm ◽  
Diagnostic Approaches ◽  
Final Histological Diagnosis

The case presented here illustrates a 75 year old female patient who underwent surgical resection of a right adrenal mass of uncertain nature. The final histological diagnosis was consistent with leiomyosarcoma arising from the adrenal anatomic site. Primary leiomyosarcoma of the adrenal gland is a very rare malignant mesenchymal neoplasm: to our knowledge, this is only the twelfth case reported in literature. We describe the clinical course and a brief review of clinical and histological features, biologic behaviour, diagnostic approaches and therapeutic strategies.

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