scholarly journals Lichen Aureus with Dermoscopic Findings: A case report

2020 ◽  
Vol 1 (3) ◽  
pp. 121-124
Author(s):  
Gökçen ÇELİK ◽  
Havva Hilal AYVAZ ÇELİK ◽  
Seda ATAY ◽  
Halit ÜNER
Keyword(s):  
Young Adults ◽  
Case Report ◽  
Female Patient ◽  
Rare Variant ◽  
Lower Extremities ◽  
Punch Biopsy ◽  
Color Patch ◽  
Brownish Yellow ◽  
Clinicopathologic Findings ◽  
Hemosiderin Deposits

Lichen aureus is a rare variant of pigmented purpuric dermatosis, which often affects young adults and is localized mainly on the lower extremities. We present here a 31-year-old female who had a solitary golden-brown-color patch on her right leg for 1 year. Punch biopsy of the lesion revealed lymphohistiocytic band-like infiltrate of the papillary dermis with erythrocyte extravasation and hemosiderin deposits. The diagnosis of Lichen aureus was made based on clinicopathologic findings. The dermoscopic findings that support this diagnosis were brownish yellow diffuse coloration of the background, round to oval red dots, globules and patches and twisted red loops. Herein, we present the dermoscopic findings of a 31-year-old female patient with a diagnosis of lichen aureus established with clinical and histopathological features. Keywords: pigmented purpuric dermatosis, lichen aureus, dermoscopy

scholarly journals Case Report: Fibrolamellar Hepatocelullar Carcinoma In A 15 Year-Old Male.

2021 ◽  
Author(s):  
Abdulwahab Alshahrani ◽  
Hisham Al Maiman ◽  
Rawan Alibrahim ◽  
Humood Alsudairi ◽  
Marooh Mnyan
Keyword(s):  
Hepatocellular Carcinoma ◽  
Young Adults ◽  
Case Report ◽  
Surgical Resection ◽  
Rare Variant ◽  
Male Patient ◽  
Fibrolamellar Hepatocellular Carcinoma

Fibrolamellar hepatocellular carcinoma (FL-HCC) is a rare variant of hepatocellular carcinoma, occurs in young adults. It presents with vague symptoms and diagnosed by imaging and biopsy. The treatment is surgery. We report a case of 15 years old male patient who was diagnosed with (FL-HCC) and treated with surgical resection.

scholarly journals Ameloblastomatous Calcifying Odontogenic Cyst: Case Report

2019 ◽  
Vol 1 (Issue 1) ◽  
pp. 08-13
Author(s):  
Atousa Aminzadeh ◽  
Alireza Sadighi
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Variant ◽  
Odontogenic Cyst ◽  
Diagnosis And Treatment ◽  
Calcifying Odontogenic Cyst ◽  
Histological Characteristics ◽  
Odontogenic Lesion ◽  
Microscopic Diagnosis ◽  
Histologic Subtypes

Calcifying odontogenic cyst (COC) or calcifying cystic odontogenic tumor was first introduced in 1962 by Gorlin et al., as a possible oral counterpart of calcifying epitheliomas of Malherbe in skin. This lesion is a rare odontogenic lesion with variable clinico-histological characteristics. Three different histologic subtypes has been reported for COC. In this study we presented a female patient diagnosed with ameloblastomatous COC a very rare variant of this lesion and challenges regarding microscopic diagnosis and treatment of it is discussed.

scholarly journals Ameloblastomatous Calcifying Odontogenic Cyst: Case Report

2019 ◽  
pp. 8-13
Author(s):  
Atousa Aminzadeh ◽  
Alireza Sadighi
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Rare Variant ◽  
Odontogenic Cyst ◽  
Diagnosis And Treatment ◽  
Calcifying Odontogenic Cyst ◽  
Histological Characteristics ◽  
Odontogenic Lesion ◽  
Microscopic Diagnosis ◽  
Histologic Subtypes

Calcifying odontogenic cyst (COC) or calcifying cystic odontogenic tumor was first introduced in 1962 by Gorlin et al., as a possible oral counterpart of calcifying epitheliomas of Malherbe in skin. This lesion is a rare odontogenic lesion with variable clinico-histological characteristics. Three different histologic subtypes has been reported for COC. In this study we presented a female patient diagnosed with ameloblastomatous COC a very rare variant of this lesion and challenges regarding microscopic diagnosis and treatment of it is discussed.

scholarly journals Varicose Vein And Ecchymosis: A Case Report

10.3823/2508 ◽  
2017 ◽  
Vol 10 ◽  
Author(s):  
Ertan Yetkin ◽  
Selçuk Öztürk ◽  
Mehmet ILeri
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Clinical Practice ◽  
Female Patient ◽  
Varicose Vein ◽  
Chronic Venous Insufficiency ◽  
Venous Insufficiency ◽  
Lower Extremities ◽  
Micronized Purified Flavonoid Fraction ◽  
Flavonoid Fraction

Assessment of varicose vein and chronic venous insufficiency and making a differential diagnosis in patients suffering from a variety of sign and symptoms is sometimes a big challenge in daily clinical practice. Here, we present a female patient with varicose vein symptoms and ecchymosis on her lower extremities. Several irregular shaped ecchymotic lesions on both extremities in different stage of healing with deep purple have been treated by using micronized purified flavonoid fraction.

scholarly journals Cutaneous lymphangiectasia of the vulva secondary to pulmonary tuberculosis: a case report

2015 ◽  
Vol 1 (1) ◽  
pp. 14
Author(s):  
Savita Arya ◽  
Asha Nyati ◽  
Motilal Bunkar ◽  
Rajendra Prasad Takhar ◽  
Saroj Mirdha
Keyword(s):  
Case Report ◽  
Pulmonary Tuberculosis ◽  
Female Patient ◽  
Histopathological Examination ◽  
Skin Lesions ◽  
Punch Biopsy ◽  
Labia Majora ◽  
History Of ◽  
Uncommon Condition

<p>Cutaneous lymphangiectasia of the genitalia represent dilatation of upper dermal lymphatic’s following damage to previously normal deep lymphatics, is an uncommon condition and only few cases have been reported following pulmonary tuberculosis. Here we are describing a case of 75 years old female patient, who came with multiple translucent papulovesicular lesions over the vulva, labia majora, minora and upper thigh from twelve year duration, with watery discharge since eight years. She had a history of pulmonary tuberculosis twenty years ago. The patient underwent punch biopsy of the lesion over the vulva and histopathological examination confirmed our diagnosis as lymphangiectasia of the vulva. She was managed conservatively with anti-tubercular drugs and got relief in watery discharge and skin lesions.</p>

Myxoid atypical fibroxanthoma: a challenging diagnosis of a rare variant: Case report

2020 ◽  
pp. 399-403
Author(s):  
Nikolina Stavrinou ◽  
Stavroula Papadopoulou ◽  
Georgia Mitropoulou ◽  
Helen Trihia ◽  
Ioannis Provatas
Keyword(s):  
Case Report ◽  
Rare Variant ◽  
Atypical Fibroxanthoma

Verrucous Psoriasis Successfully Treated with Ixekizumab: A Case Report with Review Literature

2020 ◽  
Vol 103 (9) ◽  
pp. 948-951
Keyword(s):  
Mycobacterium Tuberculosis ◽  
Case Report ◽  
Rare Variant ◽  
Psoriasis Vulgaris ◽  
Review Literature ◽  
Antituberculous Therapy ◽  
Plaque Type ◽  
History Of

Verrucous psoriasis is a rare variant of plaque-type psoriasis with only about 35 cases reported. The authors reported a man with a history of psoriasis vulgaris for seven years, presented with progressive verrucous hyperkeratotic plaques on both legs for three years. His earlier investigations favored the diagnosis of tuberculosis verrucosa cutis. After completing the antituberculous therapy, the lesions persisted. The later investigations favored a rare subtype of psoriasis named verrucous psoriasis. Keywords: Verrucous psoriasis, Tuberculosis verrucosa cutis, Mycobacterium tuberculosis, Ixekixumab

Healing Of A Large Osteolytic Mandibular Lesion – A Case Report

2018 ◽  
Author(s):  
Ingrid Różyło-Kalinowskav ◽  
Karolina Sidor
Keyword(s):  
Case Report ◽  
Female Patient ◽  
Surgical Approach ◽  
Orthodontic Treatment ◽  
Incidental Finding ◽  
Osteolytic Lesion ◽  
Panoramic Radiograph ◽  
Endodontic Treatment ◽  
Osteolytic Lesions

The purpose of this article was to present a case report of 11–year old female patient with a large osteolytic mandibular lesion which healed after endodontic treatment. The patient was referred for radio diagnostics due to an incidental finding of a large osteolytic lesion of the area of the left lower first and second premolars in the panoramic radiograph taken before orthodontic treatment. CBCT was performed and the patient asked to have teeth 33-35 treated by endodontics before surgery. The patient missed the surgical appointment and when she reappeared several months later, the lesion showed signs of healing thus surgery were aborted. The presented case testifies to the observation that even large osteolytic lesions can heal after endodontic treatment without surgical approach.

Atypical pilocytic astrocytoma of adult spinal cord: A case report

2018 ◽  
pp. 1-2
Keyword(s):  
Spinal Cord ◽  
Young Adults ◽  
Case Report ◽  
Pilocytic Astrocytoma ◽  
Treatment Protocol ◽  
Pilomyxoid Astrocytoma ◽  
Standardized Treatment ◽  
Children And Young Adults ◽  
Adult Spinal Cord

Pilomyxoid astrocytoma (PMA) is an atypical subtype of pilocytic astrocytoma (PA), which presents in children and young adults. The incidence of PMA is low, so there is no standardized treatment protocol for it. Here, we present a 62-year-old woman with recurrent PMA, which is important for the understanding and treatment of the disease.

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