Vascular Tumors

Vascular Tumors of Skin (31 cases in 3 hours): Board Review for Pathology Dermatology Dermpath
Vascular Tumors of Skin (31 cases in 3 hours): Board Review for Pathology Dermatology Dermpath administrator 7 Views • 2 years ago

Vascular tumors of skin board review for pathology, dermatology, and dermatopathology. 31 cases in 3 hours. Enjoy!

Links and info referenced in video available here:
https://kikoxp.com/posts/28968

List of entities discussed (click timestamp to go to that part of video):

1. Targetoid hemosiderotic hemangioma 0:18
What does hobnail mean? 3:27 – 5:01
2. Glomus tumor 7:53
3. Tufted angioma / Kaposiform Hemangioendothelioma 12:42
4. Angiosarcoma 18:13
5. Angioleiomyoma (leiomyoma, vascular type) 24:11
6. Nodular Kaposi sarcoma 28:08
7. Glomeruloid hemangioma 36:54
8. Erythema elevatum diutinum (EED) 38:43
9. Pyogenic granuloma 43:27
10. “Masson Tumor” Intravascular papillary endothelial hyperplasia (IPEH) 46:29
11. Angiokeratoma 52:10
12. Epithelioid hemangioma/angiolymphoid hyperplasia with eosinophilia (ALHE) 56:04
13. Solar purpura 1:01:19
14. Hidradenoma (Acrospiroma) 1:04:38
15. Venous Stasis vascular change 1:11:09
16. Hibernoma 1:14:37
17. Post radiation angiosarcoma & Severe post-radiation changes 1:21:36
18. Glomangioma 1:27:56
19. Polypoid Dermatofibroma, aneurysmal type “sclerosing hemangioma” type 1:31:24
20. Patch Kaposi sarcoma 1:36:49
21. Lymphangioma 1:45:42
22. Verrucous hemangioma 1:51:31
23. AV hemangioma 1:55:35
24. Spindle cell hemangioma 1:57:58
25. Superficial angiomyxoma 2:08:00
26. Venous lake 2:19:17
27. Infantile hemangioma 2:22:11
28. Temporal arteritis 2:27:46
29. Microvenular hemangioma 2:31:53
30. Thrombus 2:36:07
31. Cavernous hemangioma (vascular malformation) vs Eccrine angiomatous hamartoma 2:39:13
Mucin around eccrine coils 2:43:27


A complete organized library of all my videos, digital slides, pics, & sample pathology reports is available here: https://kikoxp.com/posts/5084 (dermpath) & https://kikoxp.com/posts/5083 (bone/soft tissue sarcoma pathology).

You might like my Twitter/social media 101 guide: https://kikoxp.com/posts/15217

Please check out my Soft Tissue Pathology & Dermatopathology survival guide textbooks. A look inside & info about where to buy them here: https://kikoxp.com/posts/17787

Presented by Jerad M. Gardner, MD. Please subscribe to my channel to be notified of new pathology teaching videos.

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(vascular intermediate set 30 - 4/2023)

Hemangiomas : Pathology,Pathogenesis,Types of Hemangiomas ,Clinical features,Diagnosis and Treatment
Hemangiomas : Pathology,Pathogenesis,Types of Hemangiomas ,Clinical features,Diagnosis and Treatment administrator 13 Views • 2 years ago

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Hemangiomas: Pathology,Pathogenesis,Types of Hemangiomas ,Clinical features, Diagnosis and Treatment

Vascular lesions of infants and children are classified into two major types: tumors and vascular malformations .Infantile hemangiomas are the most common vascular tumors . Other examples of vascular tumors include pyogenic granuloma, kaposiform hemangioendothelioma, and tufted angioma. So-called rapidly involuting (RICH) and non-involuting (NICH) "congenital" hemangiomas appear histopathologically to be hybrids showing features of both vascular tumor and malformation. Because cases of RICH evolving into NICH have been reported, it has been suggested that these two entities lie within the same spectrum.
• Hemangiomas are the most common tumors of infancy. The true incidence of infantile hemangiomas is unknown. Although they are classically said to occur in up to 10 percent of Caucasian infants, 4 to 5 percent is probably a better estimate. Infantile hemangiomas are generally noticed within the first few days to months of life . Although most hemangiomas occur sporadically, familial transmission in an autosomal dominant fashion has been reported. In one series of 136 patients/families, 34 percent had a family history of infantile hemangiomas, most often in first-degree relatives

Epidemiology

• The majority of hemangiomas are not clinically evident at birth but become apparent within the first days to months of life. Some newborns have a premonitory cutaneous mark, such as a patch of telangiectasia’s with surrounding pallor (secondary to vasoconstriction) at the hemangioma site. Early lesions may be so subtle as to go unrecognized and may be mistaken for a scratch or bruise. Less commonly, a hemangioma may appear initially as a bright red patch resembling a port-wine stain.
• The majority of lesions are solitary, but multiple lesions occur in up to 20 percent of infants and are especially common among multiple births. Hemangiomas have a predilection for the head and neck, although they can occur anywhere in the skin, mucous membranes, or internal organs. Hemangiomas range in size from a few millimeters to many centimeters in diameter. They may be superficial, deep, or combined (compound hemangioma).

Clinical features

• The superficial presentation is most common and consists of a bright red papule, nodule, or plaque raised above clinically normal skin. Superficial hemangiomas have been called "strawberry" or "capillary" hemangiomas, but superficial hemangioma is the preferred term, since not all superficial hemangiomas have the "strawberry" appearance, and not all strawberry-like lesions are hemangiomas .

• The deep, or subcutaneous, hemangioma is typically a raised, skin-colored nodule, which often has a bluish hue with or without central telangiectatic patch. Purely deep hemangiomas are less common. They have been called "cavernous" hemangiomas, a term that is also erroneously used to describe venous malformations and thus is best avoided.
• Combined hemangiomas are common and contain both superficial and deep components.

Complication

• Most cutaneous hemangiomas are uncomplicated and require no intervention. However, some lesions may ulcerate, leading to pain, bleeding, scarring, and/or infection. Other lesions may cause functional impairment during, and/or disfigurement after, the proliferative phase
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Vascular Pathology -  Robbins Pathology - Chapter 4
Vascular Pathology - Robbins Pathology - Chapter 4 administrator 4 Views • 2 years ago

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🩸🛤️ Unraveling Vascular Pathology: Vasculitis & Atherosclerosis! 📚🔬 Pathology Chapter - 4 🧠💉

Description:
Welcome to Chapter 4 of our enthralling Pathology series! 🎉 In this installment, we're delving deep into the captivating world of Vascular Pathology, focusing on two intriguing conditions: Vasculitis and Atherosclerosis. 🤩🔍

🩸 Vasculitis: The Inflammatory Odyssey 🌪️🚩
Join us on a journey through the enigmatic realm of Vasculitis, a group of inflammatory diseases that affect blood vessels. 🛣️💥 We'll explore the various types of Vasculitis, their clinical presentations, and the underlying mechanisms that lead to these fascinating conditions. 🕵️‍♂️🧬 Prepare to be amazed as we unravel the mysteries behind this complex disorder! 😲🕵️‍♀️

🛤️ Atherosclerosis: The Silent Culprit 🏰💔
Discover the stealthy intruder of the cardiovascular system - Atherosclerosis! 🦠🏢 We'll investigate how this progressive disease silently wreaks havoc within our arteries, leading to plaque formation and potential life-threatening consequences. 💔⚠️ Learn about risk factors, prevention strategies, and the latest research on combatting this deadly menace. 💪🔬

📚 Chapter 4 of our Pathology series promises to be an eye-opening and informative experience! 🌟📖 Whether you're a medical student, healthcare professional, or simply curious about the inner workings of the human body, this video is a must-watch! 🩺🤓

🔥🧭 Don't forget to like, share, and subscribe to our channel to stay tuned for more captivating journeys through the realm of medicine and pathology! 📺🤗

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Vascular tumors - Angiosarcoma - Definition, Epidemiology, Pathology, Diagnosis and treatment
Vascular tumors - Angiosarcoma - Definition, Epidemiology, Pathology, Diagnosis and treatment administrator 4 Views • 2 years ago

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Vascular tumors - Angiosarcoma - Definition, Epidemiology, Pathology, Diagnosis, and treatment

Angiosarcomas are uncommon malignant neoplasms of vascular endothelial cell origin. They may arise at a number of different body sites, but the most common form of angiosarcoma, Wilson-Jones angiosarcoma, occurs in the head and neck region of elderly individuals.

There is a strong male preponderance. Risk factors for the development of angiosarcoma include the history of radiotherapy, foreign materials (eg, shrapnel, steel, plastic, Dacron) in the body, chronic lymphedema, and environmental agents such as arsenic and vinyl chloride.

Angiosarcomas are aggressive tumors that tend to grow rapidly, recur locally, and metastasize widely. Prognosis is poor; five-year survival rates are less than 20%. This is due to the biologic behavior of the tumor as well as delays in diagnosis. Initially, lesions may mimic ecchymoses or cellulitis. Medical personnel should maintain a high degree of suspicion and inquire about systemic signs of malignancy (eg, weight loss, fatigue, mass).

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