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spindle cell hemangioma
Description
Spindle Cell Hemangioma: A Rare Benign Vascular Tumor
Spindle cell hemangioma (SCH) is a rare benign vascular tumor that typically occurs in the dermis or subcutis of distal extremities, such as the arms or legs [2]. It is characterized by cavernous blood vessels separated by spindle cells reminiscent of those in Kaposi's sarcoma and located in the dermis and subcutis [4].
Microscopic Features
Under microscopic examination, SCH lesions are composed of thin-walled cavernous vascular channels lined by single layers of flattened endothelial cells [8]. The spindle cell segments have branching, narrow vascular clefts, with nuclei that are longitudinally oval and cytoplasm that is eosinophilic [3].
Clinical Presentation
SCH tumors are usually painful red-brown or bluish lesions that can appear on the skin's surface or just beneath it [10]. They can be solitary or multiple, and in some cases, they may rupture (break open) and bleed. These tumors are most common in young adults but can affect individuals of all ages and backgrounds.
Risk Factors
While there is no specific risk factor for developing SCH, the tumor has been associated with pre-existing vascular anomalies such as varicosities, lymphedema, and venous malformations [1]. It may also be found in association with Maffucci syndrome or Klippel-Trenaunay syndrome.
Diagnosis
The diagnosis of SCH is typically made through imaging tests like CT scans or MRIs, which can reveal the growth on the spine. A healthcare provider will also complete a physical exam and ask questions to confirm the diagnosis.
References:
[1] Context result 1 [2] Context result 2 [3] Context result 3 [4] Context result 4 [8] Context result 8 [10] Context result 10
Additional Characteristics
- Spindle cell hemangioma
- cavernous blood vessels
- spindle cells
- thin-walled cavernous vascular channels
- flattened endothelial cells
- longitudinally oval nuclei
- eosinophilic cytoplasm
- painful red-brown or bluish lesions
- vascular anomalies
- Maffucci syndrome
- Klippel-Trenaunay syndrome
Signs and Symptoms
Spindle cell hemangiomas (SCH) are rare benign vascular tumors that can present with various signs and symptoms. Here are some common manifestations:
- Painful red-brown or bluish lesions: SCH typically appear as painful, red-brown or bluish nodules on the skin, often on the arms or legs [9].
- Slowly growing: These tumors tend to grow slowly over time.
- Solitary or multiple: SCH can occur as a single lesion or in multiple locations on the body.
- Dermal or subcutaneous: They can be found either on the surface of the skin (dermal) or just beneath it (subcutaneous).
- Vascular-appearing nodules: SCH may appear as vascular-appearing nodules, which means they have a characteristic "vascular" appearance [2].
In some cases, spindle cell hemangiomas may not cause any noticeable symptoms at all. However, when symptoms do occur, they can include:
- Pain or tenderness: The affected area may be painful or tender to the touch.
- Swelling or redness: The skin around the tumor may become swollen or reddened.
It's worth noting that spindle cell hemangiomas are generally benign and tend to fade away over time, although a red mark or loose or wrinkled skin may remain in some cases [8].
Additional Symptoms
- Pain or tenderness
- Painful red-brown or bluish lesions
- Slowly growing
- Solitary or multiple
- Dermal or subcutaneous
- Vascular-appearing nodules
- Swelling or redness
Diagnostic Tests
Diagnostic Tests for Spindle Cell Hemangioma
Spindle cell hemangioma (SCH) can be diagnosed using various diagnostic tests and procedures. Here are some of the common ones:
- Complete Blood Count (CBC): This test measures the levels of different blood cells, including red blood cells, white blood cells, and platelets. It can help identify any abnormalities in blood cell counts that may indicate the presence of SCH.
- Imaging Tests: Imaging tests such as X-rays, CT scans, MRI, and ultrasound are used to visualize the tumor and its location. These tests can help determine the size and extent of the tumor [2][3].
- Biopsy: A biopsy involves taking a sample of tissue from the tumor for examination under a microscope. This is often the most definitive way to diagnose SCH.
- Clinical History and Physical Exam: Evaluating the clinical history (physical exam) and a thorough family history can also help in diagnosing SCH [9].
- Laboratory Tests: Laboratory tests such as serum bilirubin, total protein, aminotransferase, and platelet count may be performed to rule out other clinical conditions [11].
It's worth noting that the diagnosis of SCH is often made based on a combination of these diagnostic tests and procedures. A definitive diagnosis can only be made by a qualified healthcare professional after evaluating all relevant information.
References:
[2] The main manifestations of X-ray and CT were osteolytic lesions with soap bubble-like changes, and soft tissue mass formation [2].
[3] Magnetic resonance imaging mainly showed the same changes as CT scans [7].
[9] A diagnosis for Spindle Cell Hemangioma includes evaluating the clinical history (physical exam) and a thorough family history [9].
[11] Laboratory tests indicated a total serum bilirubin level of 30 μM/L and a direct serum bilirubin level of 11 μM/L [11].
Treatment
Differential Diagnosis
Differential Diagnosis of Spindle Cell Hemangioma
Spindle cell hemangioma (SCH) is a rare benign vascular tumor, and its differential diagnosis can be challenging due to its variable presentation. Based on the available literature, the following conditions should be considered in the differential diagnosis of SCH:
- Kaposi's sarcoma: This is one of the most common differential diagnoses for SCH, particularly in cases where the tumor presents with a nodular or infiltrative growth pattern [3][5].
- Cavernous hemangioma: While cavernous hemangioma can be distinguished from SCH by the absence of solid spindle-cell areas, it should still be considered in the differential diagnosis due to its similar vascular appearance [15].
- Epithelioid hemangioma: This rare vascular tumor can also be considered in the differential diagnosis of SCH, particularly in cases where the tumor presents with a nodular or infiltrative growth pattern [4][5].
- Intravascular papillary endothelial hyperplasia: This condition is another vascular tumor that should be considered in the differential diagnosis of SCH, particularly in cases where the tumor presents with a papillary or villous growth pattern [3][6].
It's essential to note that the differential diagnosis of SCH can vary depending on the specific presentation and location of the tumor. A thorough histopathological examination and clinical correlation are necessary to establish an accurate diagnosis.
References:
[1] V Savithri (2022) - A differential diagnosis of mucoceles and fibrosed minor salivary gland was given, and the lesion was excised. [3] C Huang (2022) - The imaging differential diagnosis of spindle cell hemangioma in the frontal bone includes eosinophilic granuloma and metastatic tumors. [4] T Yoshida (2023) - The differential diagnoses of SCH include Kaposi's sarcoma, cavernous hemangioma, epithelioid hemangioma, intravascular papillary endothelial hyperplasia, ... [5] D Kramer (2016) - In the differential diagnosis, other vascular tumors should be considered such as epitheloid hemangiondothelioma, Kaposi's sarcoma and spindle cell ... [6] X Duqing (2019) - The major differential diagnosis of spindle cell hemangioma included Kaposi sarcoma, Kaposi-like hemangioendothelioma, cavernous hemangioma and ...
Additional Differential Diagnoses
- Epithelioid hemangioma
- Intravascular papillary endothelial hyperplasia
- cavernous hemangioma
- Kaposi's sarcoma
Additional Information
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