CYTOPATHOLOGY AS AN IMPORTANT TOOL IN DIAGNOSING LYMPHANGIOMA CIRCUMSCRIPTUM OF BREAST – A RARE CASE REPORT.

2021 ◽  
pp. 28-29
Author(s):  
Mangesh Machindra Londhe ◽  
Tushar Vithalrao Patil ◽  
Kishor H Suryawanshi ◽  
Priyanka Sunil Gaikwad
Keyword(s):  
Case Report ◽  
Vascular Malformation ◽  
Crucial Role ◽  
Rare Case ◽  
Accurate Diagnosis ◽  
Unique Case ◽  
Surgical Exploration ◽  
Rare Case Report ◽  
Lymphangioma Circumscriptum

Lymphangiomas of breast are rare with only a few cases being reported so far. Among these secondary lymphangioma have been reported but cases of primary lymphangioma are even rarer. Due to its proclivity to mimic malignancy clinically, its accurate diagnosis plays a crucial role in management of these patients. This is a unique case where cytology suggested a diagnosis of vascular malformation ruling out malignancy, thus avoiding unnecessary surgical exploration along with untoward effects of chemo/radiotherapy. The histopathology revealed diagnosis of lymphangioma circumscriptum of breast

Intramuscular vascular malformation of the masseter: a rare case report

1996 ◽  
Vol 19 (4) ◽  
pp. 221-221
Author(s):  
N. Kostakoğlu ◽  
A. Kayikcioğlu ◽  
K. G. Gürsu
Keyword(s):  
Case Report ◽  
Vascular Malformation ◽  
Rare Case ◽  
Rare Case Report

Lymphangioma circumscriptum of the vulva: a rare case report

2012 ◽  
Vol 165 (1) ◽  
pp. 131-132 ◽  
Author(s):  
Tasneem Nishah Shah ◽  
Sunita Shekokar ◽  
Shreedhar Venkatesh ◽  
K.V. Santosh ◽  
K.V. Santosh
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report ◽  
Lymphangioma Circumscriptum

scholarly journals Klippel Trenaunay Syndrome: a rare case report in a neonate

2016 ◽  
Vol 4 (1) ◽  
pp. 294
Author(s):  
Krishnappa Santosh Kumar ◽  
Nanjappa Mohan Kumar
Keyword(s):  
Case Report ◽  
Soft Tissue ◽  
Vascular Malformation ◽  
Conservative Management ◽  
Rare Case ◽  
Lymphatic Malformation ◽  
Rare Case Report ◽  
Klippel Trenaunay Syndrome ◽  
Prompt Diagnosis

Klippel Trenaunay Syndrome (KTS) is a cutaneous vascular malformation in combination with bone and soft tissue overgrowth, with or without lymphatic malformation. Symptoms appear by birth and approximately 90% of the cases are diagnosed by the age of 12 years. Prompt diagnosis at the earliest and conservative management with regular follow up is crucial in prognosis of KTS.

scholarly journals Triple-component Mixed Neuroendocrine-Nonneuroendcocrine Neoplasm of the duodenum: A rare case report

2021 ◽  
Author(s):  
Souhir Khemiri ◽  
Sonda Masmoudi ◽  
Asma Yaich ◽  
Ons Boudawara ◽  
Samir Aloulou ◽  
...  
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Cell Carcinoma ◽  
Neuroendocrine Tumor ◽  
Squamous Cell ◽  
Rare Case ◽  
Neuroendocrine Neoplasms ◽  
Unique Case ◽  
Rare Case Report

Mixed neuroendocrine-non-neuroendocrine neoplasms (MiNEN) are an heterogeneous subgroup of rare neoplasms. Triple componed MiNEN associating neuroendocrine tumor, adenocarcinoma and squamous cell carcinoma are rarely described in the literature. Here we present the unique case of a 56-year-old women with neuroendocrine tumor, adenocarcinoma and squamous cell carcinoma of the duodenum

scholarly journals Ameloblastic Carcinoma with Calcification: A Rare Case Report in the Mandible and Literature Review

2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Neda Kardouni Khoozestani ◽  
Farzaneh Mosavat ◽  
Mohammad Shirkhoda ◽  
Ramtin Azar
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Age Groups ◽  
Accurate Diagnosis ◽  
Dystrophic Calcification ◽  
Ameloblastic Carcinoma ◽  
Wide Range ◽  
Rare Case Report ◽  
Microscopic Features ◽  
Treatment Plans

Ameloblastic carcinoma (AC) is a scarce malignant tumor which is more prevalent in the mandible than the maxilla. It occurs in a wide range of age groups, and there is a sex predilection in males. AC shows specific microscopic features and requires more aggressive surgical treatment plans in comparison with conventional ameloblastoma. Radiographically, AC resembles ameloblastoma except that it rarely represents focal mineralized materials, seemingly reflecting dystrophic calcification. This characteristic is uncommon in typical ameloblastomas, and only few cases reported with such opacities and mineralized materials. Due to this rare radiographic and microscopic presentation, an accurate diagnosis could be challenging, and pathologists should consider a combination of benign and malignant odontogenic tumors occurring in jaws.

Acquired lymphangioma circumscriptum secondary to tuberculosis: A rare case report

2020 ◽  
Vol 33 (4) ◽  
Author(s):  
Fariba Ghalamkarpour ◽  
Zahra Asadi‐kani ◽  
Afshin Moradi ◽  
Shirin Zaresharifi ◽  
Pegah Khazaei
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Rare Case Report ◽  
Lymphangioma Circumscriptum

scholarly journals Schwannoma of the infratemporal fossa - A rare case report

2020 ◽  
Vol 75 (9) ◽  
pp. 485-487
Author(s):  
Shivani Bansal ◽  
Dilipkumar Basavanthappa ◽  
Pooja Prasad ◽  
Mugdha S Raut ◽  
Rajiv S Desai
Keyword(s):  
Differential Diagnosis ◽  
Case Report ◽  
Rare Case ◽  
Infratemporal Fossa ◽  
Facial Asymmetry ◽  
Accurate Diagnosis ◽  
Head And Neck Tumours ◽  
Nerve Sheath Tumour ◽  
Nerve Sheath ◽  
Rare Case Report

Schwannoma is a benign nerve sheath tumour that originates from schwann cells of the peripheral nerve. In spite of constituting 25-40% of head and neck tumours its in-traoral presentation is rare which accounts for only 1%. The purpose of this case report is to highlight the rarity of this lesion, to emphasize the significance of an accurate diagnosis and to include tumours of nerve sheath origin in the differential diagnosis of facial asymmetry.

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